Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the <it>MYBPC3 </it>gene

<p>Abstract</p> <p>Background</p> <p>Mutations in <it>MYBPC3 </it>encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). <it>MYBPC3 </it>mutatio...

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Bibliographic Details
Main Authors: Lehrke Stephanie, Zeller Raphael, Pribe Regina, Steen Henning, Zehelein Jörg, Weichenhan Dieter, Ehlermann Philipp, Zugck Christian, Ivandic Boris T, Katus Hugo A
Format: Article
Language:English
Published: BMC 2008-10-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/9/95