Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.
第一作者:
Ghayath,Baroudi
第一单位:
Department of Medicine, Laval University, Québec Heart Institute and Research Centre, Laval Hospital, Sainte-Foy.
作者:
主题词
成年人(Adult);束支传导阻滞(Bundle-Branch Block);密码子, 无义(Codon, Nonsense);除颤器, 植入型(Defibrillators, Implantable);超声心动描记术(Echocardiography);电抗休克(Electric Countershock);心电描记术(Electrocardiography);女(雌)性(Female);遗传标记(Genetic Markers);疾病遗传易感性(Genetic Predisposition to Disease);心脏传导系统(Heart Conduction System);人类(Humans);男(雄)性(Male);显微镜检查, 共焦(Microscopy, Confocal);中年人(Middle Aged);突变, 误义(Mutation, Missense);膜片钳术(Patch-Clamp Techniques);表型(Phenotype);钠通道(Sodium Channels);统计学(主题)(Statistics as Topic);综合征(Syndrome);心室颤动(Ventricular Fibrillation)
PMID
15057319
发布时间
2025-05-29
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