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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Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi Publishing Corporation 2013
Onderwerpen:
Clinical Study
Online toegang: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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