A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.
第一作者:
Morten Salling,Olesen
第一单位:
The Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark. morten.salling.olesen@rh.regionh.dk
作者:
主题词
成年人(Adult);发病年龄(Age of Onset);动物(Animals);心房颤动(Atrial Fibrillation);CHO细胞(CHO Cells);病例对照研究(Case-Control Studies);仓鼠亚科(Cricetinae);仓鼠属(Cricetulus);丹麦(Denmark);心电描记术(Electrocardiography);女(雌)性(Female);遗传关联研究(Genetic Association Studies);疾病遗传易感性(Genetic Predisposition to Disease);人类(Humans);Kv通道调节蛋白质类(Kv Channel-Interacting Proteins);男(雄)性(Male);膜电位(Membrane Potentials);突变(Mutation);表型(Phenotype);钾(Potassium);Shal钾通道(Shal Potassium Channels);转染(Transfection);青年人(Young Adult)
DOI
10.1093/cvr/cvt028
PMID
23400760
发布时间
2013-05-20
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Cardiovascular research
488-95页
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