Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.

Circulation. Cardiovascular genetics

PubMedID: 27418595

LaHaye S, Corsemeier D, Basu M, Bowman JL, Fitzgerald-Butt S, Zender G, Bosse K, McBride KL, White P, Garg V. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. Circ Cardiovasc Genet. 2016;.
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