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遗传性室性心律失常的基因、分子电生理及临床 被引量：1

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作者 王洪涛 刘同库 浦介麟
机构地区 中国医学科学院阜外心血管病医院心律失常诊治中心分子病理生理实验中心 北华大学附属医院心内科
出处 《中华内科杂志》 CAS CSCD 北大核心 2006年第4期341-343,共3页 Chinese Journal of Internal Medicine
基金 国家自然科学基金资助项目(30270556)
关键词 遗传性室性心律失常 离子通道基因 分子生物学 临床特点 电生理 心律失常相关基因 机制研究 身体健康 突变
分类号 R541.7 [医药卫生—心血管疾病] R742.1 [医药卫生—神经病学与精神病学]
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参考文献28

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二级参考文献75

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共引文献1

同被引文献4

  • 1Wang Q, chen Q, Towbin JA. Genetics, molecular mechanisms and management of long QT syndrome. Ann Med, 1998,30:58-65
  • 2Schwartz PJ, Priori SG, Spazzolini C, et al. Genotype-phenotype correlation in the long-QT syndrome:gene-specific triggers for life threatening arrhythmias. Circulation, 2001,103 : 89 -95
  • 3Splawski I, Timothy KW, Sharpe LM, et al. Ca(V) 1,2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. Cell ,2004,119 : 19-31
  • 4Wilde AA, Antzelevitch C, Borggrefe M, et al, Proposed diagnostic criteria for the Brugada syndrome Eur Heart J,2002, 23 : 1648-1654

引证文献1

中华内科杂志
2006年 第4期

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