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关于《遗传性长QT综合征伴低钾血症的一家系调查》读后的一点观点 被引量:2

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作者 浦介麟 李宁
出处 《中国心脏起搏与心电生理杂志》 2005年第5期424-424,共1页 Chinese Journal of Cardiac Pacing and Electrophysiology
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  • 1Tawil R,Ptacek LJ,Pavlakis SG,et al.Andersen′s syndrome:Potassium-sensitive periodic paralysis,ventricular ectopy,and dysmorphic features[J],Ann Neurol,1994,36(2):252
  • 2Sansone V,Griggs RC,Meola G,et al.Andersen′s syndrome:A distinct periodic paralysis[J].Am Neurol,1997,42(3):305
  • 3Plaster NM,Tawil R,Tristani-Firouzi M,et al.Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen′s syndrome[J].Cell,2001,105(4):511
  • 4Tristan-Firouzi M,Jensen JL,Donaldson MR,et al.Functional and clinical characterization of KCNJ2 mutations associated with LQT7(Andersen syndrome)[J].J Clin Invest,2002,110(3):381
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  • 6Zhang L,Timothy KW,Vincent GM.Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome:ECG findings identify genotypes[J].Circulation,200,102(23):2 849
  • 7Zhang L,Benson DW,Tristani-Firouzi M,et al.Electrocardiographic featrures in Andersen-Tawil syndrom patients with KCNJ2 mutations:Characteristic T-U-wave patterns predict the KCNJ2 genotype[J].Circulation,2005,111(2):2 720

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