A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation

BACKGROUND: Atrial fibrillation (AF) is the most common cardiac arrhythmia, and its incidence is expected to grow. A genetic predisposition for AF has long been recognized, but its manifestation in these patients likely involves a combination of rare and common genetic variants. Identifying genetic...

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Huvudupphovsmän: Bartos, Daniel C., Anderson, Jeffrey B., Bastiaenen, Rachel, Johnson, Jonathan N., Gollob, Michael H, Tester, David J., Burgess, Don E., Homfray, Tessa, Behr, Elijah R., Ackerman, Michael J., Guicheney, Pascale, Delisle, Brian P.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2013
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3640728/
https://ncbi.nlm.nih.gov/pubmed/23350853
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jce.12068
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