Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathySharie B. Parks, Ray E. Hershberger, Duanxiang Li et al.|American Heart Journal|2008Cited by 256
Coding Sequence Mutations Identified in <i>MYH7, TNNT2, SCN5A, CSRP3, LBD3</i>, and <i>TCAP</i> from 313 Patients with Familial or Idiopathic Dilated CardiomyopathyRay E. Hershberger, M. Litt, Sharie B. Parks et al.|Clinical and Translational Science|2008Cited by 194
Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart FailureDuanxiang Li, Ray E. Hershberger, M. Litt et al.|The American Journal of Human Genetics|2006Cited by 183