Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects

Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects

There is strong evidence for a genetic contribution to non-syndromic congenital heart defects (CHDs). However, exome- and genome-wide studies conducted at the variant and gene-level have identified few genome-wide significant CHD-related genes. Gene-set analyses are a useful complement to such studi...

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Bibliographic Details
Main Authors: Fadi I. Musfee, A. J. Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E. Morrow, Deanne M. Taylor, Martin Tristani-Firouzi, W. Scott Watkins, Mark Yandell, Laura E. Mitchell
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Genes
Subjects:
association
case-control
case-parent trios
congenital
conotruncal
heart
Online Access:https://www.mdpi.com/2073-4425/12/5/655

Internet

https://www.mdpi.com/2073-4425/12/5/655

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