期刊文献+

从遗传性心律失常的研究中我们学到了什么

What Have We Learnt from Research of Inherited Arrhythmias
下载PDF
导出
作者 浦介麟
出处 《心血管病学进展》 CAS 2010年第1期1-3,共3页 Advances in Cardiovascular Diseases
  • 相关文献

参考文献7

  • 1Wang Q,Shen J,Splawski I,et al. SCNSA mutations associated with an inherited cardiac arrhythmia,long QT syndrome[ J ]. Cell, 1995 ,80(5 ) :805-811.
  • 2Webster G, Berul CI. Congenital long-QT syndromes:a clinical and genetic update from infancy through adulthood [ J ]. Trends Cardiovase Med ,2008,18 (6) : 216-224.
  • 3Antzelevitch C, Pollevick GD, Cordeiro JM,et al. Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST- segment elevation, short QT intervals, and sudden cardiac death [ J ]. Circulation, 2007,115(4) :442-449.
  • 4Chen YH,Xu SJ,Bendahhou S,et al. KCNQ1 gain-of-function mutation in familial atrial fibrillation [ J ]. Science,2003,299:251.
  • 5Zhang X,Chen S,Yoo S,et al. Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death [ J ]. Cell ,2008,135 (6) :1017-1027.
  • 6Bezzina CR, Shimizu W, Yang P, et al. Common sodium channel promoter haplotype in Asian subjects underlies variability in cardiac conduction [ J ]. Circulation, 2006, 113 : 338 -344.
  • 7Modell SM, Lehmann MH. The long QT syndrome family of cardiac ion channelopathies : a HuGE review [ J ]. Genet Med, 2006,8 ( 3 ) : 143-155.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部