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Article

Myoblasts from affected and non‐affected FSHD muscles exhibit morphological differentiation defects

24 May 2008

Abstract excerpt

Facioscapulohumeral dystrophy (FSHD) is a muscular hereditary disease with a prevalence of 1 in 20,000 caused by a partial deletion of a subtelomeric repeat array on chromosome 4q. However, very little is known about the pathogenesis as well as the molecular and biochemical changes linked to the progressive muscle degeneration observed in these patients. Several studies have investigated possible...

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PMID: 18505476
DOI: 10.1111/j.1582-4934.2008.00368.x

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