Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1. (Q34389612)

1 August 2017

title

Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1. (English)

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1 August 2017

1

Martinsson T

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1 August 2017

Darin N

2

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1 August 2017

Kyllerman M

3

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1 August 2017

Oldfors A

4

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1 August 2017

Hallberg B

5

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1 August 2017

Wahlström J

6

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1 August 2017

language of work or name

English

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publication date

1 May 1999

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

64

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1 August 2017

issue

5

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1 August 2017

page(s)

1420-1426

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Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis

1 August 2017

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6 July 2018

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Hereditary inclusion body myopathy maps to chromosome 9p1-q1

6 July 2018

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Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Co-expression of multiple myosin heavy chain genes, in addition to a tissue-specific one, in extraocular musculature

6 July 2018

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6 July 2018

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6 July 2018

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Inclusion body myositis and welander distal myopathy: a clinical, neurophysiological and morphological comparison

6 July 2018

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Organization of the human skeletal myosin heavy chain gene cluster

6 July 2018

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Sporadic inclusion-body myositis and its similarities to Alzheimer disease brain. Recent approaches to diagnosis and pathogenesis, and relation to aging

6 July 2018

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"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

27 October 2018

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9 December 2018

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12 December 2020

Distal myopathy: histochemical and ultrastructural studies

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12 December 2020

Oculopharyngeal muscular dystrophy and distal myopathy. Intrafamilial difference in the onset and distribution of muscular involvement

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12 December 2020

Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome

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12 December 2020

Presence of inclusion body myositis-like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 cases

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12 December 2020

Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients

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12 December 2020

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12 December 2020

The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews

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12 December 2020

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9

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12 December 2020

Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1

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12 December 2020

Familial inclusion body myositis: Evidence for autosomal dominant inheritance

1 reference

12 December 2020

Identifiers

DOI

10.1086/302375

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1 August 2017

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1 August 2017

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