(Q28288803)

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Hereditary inclusion body myopathy maps to chromosome 9p1-q1

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title

Hereditary inclusion body myopathy maps to chromosome 9p1-q1 (English)

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main subject

Hereditary inclusion body myopathy

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5

J G Seidman

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author name string

S Mitrani-Rosenbaum

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1

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Z Argov

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2

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A Blumenfeld

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3

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C E Seidman

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4

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language of work or name

English

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publication date

January 1996

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published in

Human Molecular Genetics

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volume

5

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issue

1

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page(s)

159-163

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cites work

Inclusion body myositis: new concepts

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

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

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

retrieved

21 January 2018

Friedreich's ataxia: a defect in signal transduction?

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

Phenotypic heterogeneity in familial inclusion body myopathy.

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

The 1993-94 Généthon human genetic linkage map

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

Strategies for multilocus linkage analysis in humans

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https://api.crossref.org/works/10.1093%2FHMG%2F5.1.159

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21 January 2018

(Q28288803)

Hereditary inclusion body myopathy maps to chromosome 9p1-q1

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