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 G.; Hong, Charles C.

期刊名称Cardiogenetics
作者Wells, Quinn S.; Ausborn, Natalie L.; Funke, Birgit H.; Pfotenhauer, Jean P.; Fredi, Joseph L.; Baxter, Samantha; DiSalvo, Thomas G.; Hong, Charles C.
卷第1卷
期第1期
印刷ISSN2035-8253
电子ISSN2035-8148
文件大小449.00KB
发表时间2011-08-22
DOI10.4081/cardiogenetics.2011.e10

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