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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654283/
https://www.ncbi.nlm.nih.gov/pubmed/23710137
http://dx.doi.org/10.1155/2013/373454

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654283/
https://www.ncbi.nlm.nih.gov/pubmed/23710137
http://dx.doi.org/10.1155/2013/373454

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