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Article

X-linked dilated cardiomyopathy and the dystrophin gene.

Neuromuscular disorders : NMD - 1 Jul 1999

Ferlini A, Sewry C, Melis M A, Mateddu A, Muntoni F

Abstract excerpt

X-linked dilated cardiomyopathy (XLDC) represents a well known genetic disease, allelic to Duchenne and Becker muscular dystrophies and caused by dystrophin gene mutations. XLDC is a rare disease and only few families have been fully characterised. In several of them, the dystrophin mutations show a different pattern of expression in cardiac compared to skeletal muscle. In the families with the most severe...

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Identifiers

PMID: 10407857
DOI: 10.1016/s0960-8966(99)00015-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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