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Article

[Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)].

Rinsho shinkeigaku = Clinical neurology - 1 Dec 1995

Goto K, Song M D, Lee J H, Arahata K

Abstract excerpt

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant muscular disorder which is characterized by progressive weakness and atrophy of the facial, shoulder-girdle and upper arm muscles, and occasional subsequent pelvic-girdle and lower limb involvement. The gene responsible for FS...

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Source

Identifiers

PMID: 8752415

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-8752415-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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