Gene-Specific Therapy for Congenital Long QT Syndrome Are We There Yet?

被引：5
作者：
Arbelo, Elena [1 ]
Sarquella-Brugada, Georgia [2 ]
Brugada, Josep [1 ,2 ]
机构：
[1] Hosp Clin Barcelona, Cardiovasc Inst, Dept Cardiol, Barcelona, Spain
[2] Hosp San Joan de Deu, Dept Pediat Cardiol, Barcelona, Spain
来源：
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY | 2016年 / 67卷 / 09期
关键词：
arrhythmia; mutation; sodium-channel blocker; sudden cardiac death; NA+ CHANNEL BLOCKADE; SCN5A; MANAGEMENT; MEXILETINE; MUTATIONS; GENOTYPE; EVENTS;
D O I：
10.1016/j.jacc.2015.12.030
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：1059 / 1061
页数：3
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