Application of high-throughput sequencing for studying genomic variations in congenital heart disease.

Abstract

Congenital heart diseases (CHD) represent the most common birth defect in human. The majority of cases are caused by a combination of complex genetic alterations and environmental influences. In the past, many disease-causing mutations have been identified; however, there is still a large proportion of cardiac malformations with unknown precise origin. High… (More)
DOI: 10.1093/bfgp/elt040

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