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[KCNQ1 mutation in patients with lone atrial fibrillation].
Zhonghua Xin Xue Guan Bing Za Zhi
January 2013
Department of cardiology, Ningbo First Affiliated Hospital of the Medical College of Ningbo University, Ningbo, China.
Objective: Recent studies suggest that mutation of the slow delayed rectifier potassium channel [I(Ks)] contributes to familial atrial fibrillation (FAF). In the current study, we explored the potential association between KCNQ1 polymorphism with lone AF (LAF).
Methods: Clinical data and blood samples were collected from 95 Han Chinese patients with LAF and matched healthy controls.