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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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Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Acesso em linha: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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