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Polymorphisms but Not Mutations of the KCNQ1 Gene Are Associated with Lone Atrial Fibrillation in the Chinese Han Population

Background. Recent studies suggest that mutation of the slow delayed rectifier potassium channel (IKs) contributes to familial atrial fibrillation (FAF). In the current study, we identified common genetic variants of KCNQ1 and explored the potential association between KCNQ1 polymorphism with lone A...

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書誌詳細
主要な著者: Chu, Hui-min, Feng, Ming-jun, Li, Yi-gang, Zhang, Yi-xin, Ma, Ji-fang, He, Bin, Yu, Yi-bo, Liu, Jing, Chen, Xiao-min
フォーマット: Artigo
言語:Inglês
出版事項: Hindawi Publishing Corporation 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3654283/
https://ncbi.nlm.nih.gov/pubmed/23710137
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/373454
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