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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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: Musfee, Fadi I., Agopian, A. J., Goldmuntz, Elizabeth, Hakonarson, Hakon, Morrow, Bernice E., Taylor, Deanne M., Tristani-Firouzi, Martin, Watkins, W. Scott, Yandell, Mark, Mitchell, Laura E.
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8146932/
https://ncbi.nlm.nih.gov/pubmed/33925651
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12050655
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