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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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Clinical Study
Acesso em linha: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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