Genomic frontiers in congenital heart disease.

Pages: 1 - 17
Published: Jul 16, 2021
Abstract
The application of next-generation sequencing to study congenital heart disease (CHD) is increasingly providing new insights into the causes and mechanisms of this prevalent birth anomaly. Whole-exome sequencing analysis identifies damaging gene variants altering single or contiguous nucleotides that are assigned pathogenicity based on statistical analyses of families and cohorts with CHD, high expression in the developing heart and depletion of...
Paper Details
Title
Genomic frontiers in congenital heart disease.
Published Date
Jul 16, 2021
Pages
1 - 17
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