Associated Papers
Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.
Morales A et al.
Circulation, 2010
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
Hershberger RE et al.
Clinical and Translational Science, 2008
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