(Q24535854)

4 July 2017

0 references

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36. (English)

1 reference

4 July 2017

2 references

parkinsonian syndrome

1 reference

inferred from title

author

Cornelia M. van Duijn

1

object named as

C M van Duijn

1 reference

4 July 2017

M C Dekker

2

1 reference

4 July 2017

V Bonifati

3

1 reference

4 July 2017

R J Galjaard

4

1 reference

4 July 2017

J J Houwing-Duistermaat

5

1 reference

4 July 2017

P J Snijders

6

1 reference

4 July 2017

L Testers

7

1 reference

4 July 2017

G J Breedveld

8

1 reference

4 July 2017

M Horstink

9

1 reference

4 July 2017

L A Sandkuijl

10

1 reference

4 July 2017

J C van Swieten

11

1 reference

4 July 2017

B A Oostra

12

1 reference

4 July 2017

P Heutink

13

1 reference

4 July 2017

language of work or name

English

0 references

publication date

2 July 2001

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

69

1 reference

4 July 2017

issue

3

1 reference

4 July 2017

page(s)

629-634

1 reference

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

A simple salting out procedure for extracting DNA from human nucleated cells

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

Parkinsonism: onset, progression, and mortality

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

Association between early-onset Parkinson's disease and mutations in the parkin gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

Pitfalls in homozygosity mapping.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

The ubiquitin pathway in Parkinson's disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235491

30 May 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/11462174

12 December 2020

inferred from PubMed ID database lookup

Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11462174

12 December 2020

inferred from PubMed ID database lookup

A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F322996

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/322996

1 reference

OpenCitations bibliographic resource ID

4 July 2017

2954784

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

4 July 2017

1 reference