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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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| Main Authors: | , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| 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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