Coding Sequence Mutations Identified in <i>MYH7, TNNT2, SCN5A, CSRP3, LBD3</i>, and <i>TCAP</i> from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

Abstract

Mutations of these six genes each account for a small fraction of the genetic cause of FDC/IDC. The frequency of possible or likely disease-causing mutations in these genes is similar for IDC and FDC.