(Q39377582)

11 September 2017

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title

Twenty years since the discovery of the parkin gene (English)

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11 September 2017

1

Nobutaka Hattori

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11 September 2017

2

Yoshikuni Mizuno

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11 September 2017

publication date

15 June 2017

1 reference

Journal of Neural Transmission

11 September 2017

published in

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A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

11 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Chronic overload of SEPT4, a parkin substrate that aggregates in Parkinson's disease, causes behavioral alterations but not neurodegeneration in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Structure of phosphorylated UBL domain and insights into PINK1-orchestrated parkin activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Human BAC library: construction and rapid screening

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Human Mn superoxide dismutase cDNA sequence

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Novel parkin mutations detected in patients with early-onset Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Susceptibility to rotenone is increased in neurons from parkin null mice and is reduced by minocycline

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

SEPT5_v2 is a parkin-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Case-control study of the parkin gene in early-onset Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The Peroxisome: A New Cytoplasmic Organelle

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Targeted overexpression of the parkin substrate Pael-R in the nigrostriatal system of adult rats to model Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin-dependent degradation of the F-box protein Fbw7β promotes neuronal survival in response to oxidative stress by stabilizing Mcl-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Lewy bodies and parkinsonism in families with parkin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The mitochondrial protein BNIP3L is the substrate of PARK2 and mediates mitophagy in PINK1/PARK2 pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin promotes the ubiquitination and degradation of the mitochondrial fusion factor mitofusin 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The striatal dopaminergic deficit is dependent on the number of mutant alleles in a family with mutations in the parkin gene: evidence for enzymatic parkin function in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Identification of a novel Zn2+-binding domain in the autosomal recessive juvenile Parkinson-related E3 ligase parkin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mitochondrial dysfunction associated with increased oxidative stress and α-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Nonmotor symptoms in Parkin gene-related parkinsonism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

BAG5 inhibits parkin and enhances dopaminergic neuron degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Inhibitory PAS domain protein is a substrate of PINK1 and Parkin and mediates cell death in a Parkinson's disease model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Phosphorylation of Parkin at Serine65 is essential for activation: elaboration of a Miro1 substrate-based assay of Parkin E3 ligase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin disease: a phenotypic study of a large case series

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin is protective for substantia nigra dopamine neurons in a tau gene transfer neurodegeneration model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Guidelines for the use and interpretation of assays for monitoring autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Structural insights into Parkin substrate lysine targeting from minimal Miro substrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Accumulation of the authentic parkin substrate aminoacyl-tRNA synthetase cofactor, p38/JTV-1, leads to catecholaminergic cell death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

1-Benzyl-1,2,3,4-tetrahydroisoquinoline binds with tubulin beta, a substrate of parkin, and reduces its polyubiquitination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Ubiquitin is phosphorylated by PINK1 to activate parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin is associated with cellular vesicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Disruption of the autoinhibited state primes the E3 ligase parkin for activation and catalysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Rapid eye movement sleep behavior disorder in parkinsonism with parkin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

STEP61 is a substrate of the E3 ligase parkin and is upregulated in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The effects of oxidative stress on parkin and other E3 ligases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin mediates nonclassical, proteasomal-independent ubiquitination of synphilin-1: implications for Lewy body formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin interacts with LIM Kinase 1 and reduces its cofilin-phosphorylation activity via ubiquitination

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin variants in North American Parkinson's disease: cases and controls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin Regulates the Activity of Pyruvate Kinase M2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Common anti-apoptotic roles of parkin and alpha-synuclein in human dopaminergic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Early onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The E3 ligase parkin maintains mitochondrial integrity by increasing linear ubiquitination of NEMO

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

PINK1 is selectively stabilized on impaired mitochondria to activate Parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Unconventional PINK1 localization to the outer membrane of depolarized mitochondria drives Parkin recruitment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Phosphorylated ubiquitin chain is the genuine Parkin receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Preserved cardiac sympathetic nerve accounts for normal cardiac uptake of MIBG in PARK2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mitochondrial dysfunction and oxidative damage in parkin-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Endogenous Parkin Preserves Dopaminergic Substantia Nigral Neurons following Mitochondrial DNA Mutagenic Stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The mitochondrial fusion-promoting factor mitofusin is a substrate of the PINK1/parkin pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Reduced expression of the chaperone-mediated autophagy carrier hsc70 protein in lymphomonocytes of patients with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Decline of striatal dopamine release in parkin-deficient mice shown by ex vivo autoradiography

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

14-3-3eta is a novel regulator of parkin ubiquitin ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

A Ubl/ubiquitin switch in the activation of Parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

PINK1-mediated phosphorylation of the Parkin ubiquitin-like domain primes mitochondrial translocation of Parkin and regulates mitophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Phosphorylation of mitochondrial polyubiquitin by PINK1 promotes Parkin mitochondrial tethering

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Mn SOD activity and protein in a patient with chromosome 6-linked autosomal recessive parkinsonism in comparison with Parkinson's disease and control

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

PARIS (ZNF746) repression of PGC-1α contributes to neurodegeneration in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Early-onset Parkinson's disease in a Chinese population: 99mTc-TRODAT-1 SPECT, Parkin gene analysis and clinical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

The relation between depression and parkin genotype: the CORE-PD study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin loss leads to PARIS-dependent declines in mitochondrial mass and respiration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Familial juvenile parkinsonism: clinical and pathologic study in a family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Molecular biology of proteasomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Ubiquitin, proteasome and parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Functional modulation of parkin through physical interaction with SUMO-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin ubiquitinates and promotes the degradation of RanBP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin protects against neurotoxicity in the 6-hydroxydopamine rat model for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Drosophila overexpressing parkin R275W mutant exhibits dopaminergic neuron degeneration and mitochondrial abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin ubiquitinates Drp1 for proteasome-dependent degradation: implication of dysregulated mitochondrial dynamics in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Complex relationship between Parkin mutations and Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin mutations and early-onset parkinsonism in a Taiwanese cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Differential gene expression of HSC70/HSP70 in yellowtail cells in response to chaperone-mediated autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin gene therapy for alpha-synucleinopathy: a rat model of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00702-017-1742-7

21 January 2018

1 reference

12 December 2020

Diverse effects of pathogenic mutations of Parkin that catalyze multiple monoubiquitylation in vitro

1 reference

12 December 2020

Molecular findings in familial Parkinson disease in Spain

1 reference

12 December 2020

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27

1 reference

12 December 2020

Does parkin play a role in the peripheral nervous system? A family report

1 reference

12 December 2020

Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in Finland

1 reference

12 December 2020

Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation

1 reference

12 December 2020

1 reference

12 December 2020

Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease

1 reference

12 December 2020

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene

1 reference

12 December 2020

Heterogeneous phenotype in a family with compound heterozygous parkin gene mutations

1 reference

12 December 2020

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

1 reference

12 December 2020

Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls

1 reference

12 December 2020

Early-onset Parkinson's disease associated with a new parkin mutation in a Spanish family

1 reference

12 December 2020

Co-occurrence of restless legs syndrome andParkin mutations in two families

1 reference

12 December 2020

Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations

1 reference

12 December 2020

Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease

1 reference

12 December 2020

Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts

1 reference

12 December 2020

10.1007/S00702-017-1742-7

Identifiers

DOI

1 reference

11 September 2017

1 reference