Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene

BACKGROUND: Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine...

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Detalles Bibliográficos
Autores principales: Ehlermann, Philipp, Weichenhan, Dieter, Zehelein, Jörg, Steen, Henning, Pribe, Regina, Zeller, Raphael, Lehrke, Stephanie, Zugck, Christian, Ivandic, Boris T, Katus, Hugo A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584029/
https://www.ncbi.nlm.nih.gov/pubmed/18957093
http://dx.doi.org/10.1186/1471-2350-9-95

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584029/
https://www.ncbi.nlm.nih.gov/pubmed/18957093
http://dx.doi.org/10.1186/1471-2350-9-95

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