Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.

Ray E. Hershberger,Sharie B. Parks,Jessica D. Kushner,Duanxiang Li,Susan Ludwigsen,Petra M. Jakobs,Deirdre Nauman,Donna Burgess,Julie Partain,M. Litt

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.

2008

Ray E. Hershberger
Sharie B. Parks
Jessica D. Kushner
Duanxiang Li
Susan Ludwigsen
Petra M. Jakobs
Deirdre Nauman
Donna Burgess
Julie Partain
M. Litt

Background More than 20 genes have been reported to cause idiopathic and familial dilated cardiomyopathy (IDC/FDC), but the frequency of genetic causation remains poorly understood.

Keywords:

MYH7
Family medicine
Titin
Exon
Dilated cardiomyopathy
Mutation
Pathology
Genetics
CSRP3
Gene
Medicine
TNNT2
idiopathic dilated cardiomyopathy

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