volume 4, issue 1, Pe4333 2009
DOI: 10.1371/journal.pone.0004333
View full text
|
Sign up to set email alerts
|
Share

Abstract: Extremes of electrocardiographic QT interval are associated with increased risk for sudden cardiac death (SCD); thus, identification and characterization of genetic variants that modulate QT interval may elucidate the underlying etiology of SCD. Previous studies have revealed an association between a common genetic variant in NOS1AP and QT interval in populations of European ancestry, but this finding has not been extended to other ethnic populations. We sought to characterize the effects of NOS1AP genetic var…

Expand abstract