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Mechanisms of Disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

Arrhythmogenic right ventricular dysplasia/cardiomyopathy is an inherited cardiomyopathy estimated to affect approximately 1 in 5,000 individuals. Cardinal manifestations include right ventricular enlargement and dysfunction, fibrofatty replacement of myocytes in the right ventricle, characteristic...

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Détails bibliographiques
Auteurs principaux: Awad, Mark M, Calkins, Hugh, Judge, Daniel P
Format: Artigo
Langue:Inglês
Publié: 2008
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2822988/
https://ncbi.nlm.nih.gov/pubmed/18382419
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncpcardio1182
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