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Article

Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress.

Neuromuscular disorders : NMD - 1 May 2003

Winokur Sara T, Barrett Kathy, Martin Jorge H, Forrester James R, Simon Mariella, Tawil Rabi, Chung Seung-Ah, Masny Peter S, Figlewicz Denise A

Abstract excerpt

Facioscapulohumeral muscular dystrophy is an autosomal dominant disorder resulting from an unusual genetic mechanism. The mutation, a deletion of 3.3 kb subtelomeric repeats, appears to disrupt the regional regulation of 4q35 g ene expression. The specific gene(s)responsible for facioscapulohumeral muscular dystrophy have not been identified. However, the 'vacuolar/necrotic' phenotype exhibited by...

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PMID: 12868502
DOI: 10.1016/s0960-8966(02)00284-5

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress.PMID 12868502Read ↗

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