Genetic Variations in NOS1AP are Associated with Sudden Cardiac Death in U.S. White Community Based Populations

BACKGROUND: The electrocardiographic QT interval is associated with risk of sudden cardiac death (SCD). A previous genome-wide association study demonstrated that allelic variants (rs10494366 and rs4657139) in NOS1AP, which encodes a carboxy-terminal PDZ ligand of neuronal nitric oxide synthase, are...

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Detalhes bibliográficos
Main Authors: Kao, WH Linda, Arking, Dan E, Post, Wendy, Rea, Thomas D, Sotoodehnia, Nona, Prineas, Ronald J, Bishe, Bryan, Doan, Betty Q, Boerwinkle, Eric, Psaty, Bruce M, Tomaselli, Gordon, Coresh, Josef, Siscovick, David S, Marban, Eduardo, Spooner, Peter M, Burke, Greg L, Chakravarti, Aravinda
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2782762/
https://ncbi.nlm.nih.gov/pubmed/19204306
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCULATIONAHA.108.791723
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