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Article

Clinical, pathological, and genetic mutation analysis of sporadic inclusion body myositis in Japanese people.

Journal of neurology - 1 Sept 2012

Cai Huaying, Yabe Ichiro, Sato Kazunori, Kano Takahiro, Nakamura Masakazu, Hozen Hideki, Sasaki Hidenao

Abstract excerpt

Previous studies have identified several genetic loci associated with the development of familial inclusion body myopathy. However, there have been few genetic analyses of sporadic inclusion body myositis (sIBM). In order to explore the molecular basis of sIBM and to investigate genotype-phenotyp...

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Source

Identifiers

PMID: 22349865
DOI: 10.1007/s00415-012-6439-0

Genes

GNE
VCP

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22349865-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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