Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy
- 21 May 2008
- journal article
- Published by Wiley in Clinical and Translational Science
- Vol. 1 (1) , 21-26
- https://doi.org/10.1111/j.1752-8062.2008.00017.x
Abstract
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
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