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References

These sources were used to develop the Genetics Home Reference condition summary on DMD-associated dilated cardiomyopathy.

Beggs AH. Dystrophinopathy, the expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy. Circulation. 1997 May 20;95(10):2344-7. Review. PubMed citation
Berko BA, Swift M. X-linked dilated cardiomyopathy. N Engl J Med. 1987 May 7;316(19):1186-91. PubMed citation
Cohen N, Muntoni F. Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy. Heart. 2004 Aug;90(8):835-41. Review. PubMed citation
Ferlini A, Sewry C, Melis MA, Mateddu A, Muntoni F. X-linked dilated cardiomyopathy and the dystrophin gene. Neuromuscul Disord. 1999 Jul;9(5):339-46. Review. PubMed citation
Gene Review: Dystrophinopathies
Muntoni F, Torelli S, Ferlini A. Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet Neurol. 2003 Dec;2(12):731-40. Review. PubMed citation
Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation. 1993 Jun;87(6):1854-65. PubMed citation

Reviewed: February 2012

Published: May 20, 2013