Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant.

Wells, Quinn S; Ausborn, Natalie L; Funke, Birgit H; Pfotenhauer, Jean P; Fredi, Joseph L; Baxter, Samantha; Disalvo, Thomas D; Hong, Charles C

Wells, Quinn S; Ausborn, Natalie L; Funke, Birgit H; Pfotenhauer, Jean P; Fredi, Joseph L; Baxter, Samantha; Disalvo, Thomas D; Hong, Charles C.

Afiliação

Wells QS; Center for Inherited Heart Disease, Division of Cardiovascular Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232.

Cardiogenetics ; 1(1)2011 Aug 22.

Article em En | MEDLINE | ID: mdl-24062880

Palavras-chave

Dilated cardiomyopathy; MYBPC; Myosin binding protein C; VCL; Vinculin

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Cardiogenetics Ano de publicação: 2011 Tipo de documento: Article País de publicação: Suíça

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