Familial Dilated Cardiomyopathy caused by an Alpha-Tropomyosin Mutation: The Distinctive Natural History of Sarcomeric DCM

OBJECTIVES: To further define the role of sarcomere mutations in DCM and associated clinical phenotypes. BACKGROUND: Mutations in several contractile proteins contribute to DCM, but definitive evidence for the roles of most sarcomere genes remains limited by the lack of robust genetic support. METHO...

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Detalhes bibliográficos
Main Authors: Lakdawala, Neal, Dellefave, Lisa, Redwood, Charles S., Sparks, Elizabeth, Cirino, Allison L., Depalma, Steve, Colan, Steven D., Funke, Birgit, Zimmerman, Rebekah S., Robinson, Paul, Watkins, Hugh, Seidman, Christine E., Seidman, J. G., McNally, Elizabeth M., Ho, Carolyn Y.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3000630/
https://ncbi.nlm.nih.gov/pubmed/20117437
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2009.11.017
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