1Shimizu W, Antezelevitch C.Effects of a K + channel opener to reduce transmural dispersion of repolarization and prevent torsade de points in LQT1LQT2 and LQT3 models of the long QT syndrome [ J ]. Circulation, 2000,102:706 - 712
2Swan H, Vitassalo M, Pilppok, et al. Sinus node function and Ventricular repolarization during exercise stress test in long QT syndrome patients with KVLQTI and HERG potassium channel defects [ J ]. JACC, 1999,34: 823 -829
4Warg Q, Current ME, Splawski 1, et al. Postional cloning of a novel potassium channel gene: KVLQTI mutations cause cardiac arrhythmias [ J ] . Nat Genet, 1996,12:17 - 23
5Splawaskil, Shen J,Timofhy KW, et al. Spectrum of mutations in long QT syndrome genes: KVQTI, HERG, SCN5A, KCNE1, and KCNE2[J].Circulation,2000,102:1178- 1185
6Schwartz PJ, Moss A J, Vincent GM, et al.The long QT Syndrome:An update[J]. Circulation, 1993,88:782 - 784
7Reardon PR, matt hews BD, Scurbrough TK, et al.left thoracossopic sympatectomy and stellate ganglionectomy for treatment of the long QT syndrome [J] .Surg Endosc 2000,14:86 - 89
8Bennett PB.long QT syndrome: biophysical and pharmalologic mechanisms in LQT3[J] .J Cardiorasc Electrophysioc,2000,11:819- 822
9Khan IA. Diagnosis and Therapy of the Long QT Syndrome [ J]. Am Heart J,2002,143:7 - 14
10Jevell A, Lange- Nielsen F.Congenital deaf- mutism, functional heart disease with Prolongation of the QT interval and sudden death[ J]. Am Heart J,1957,54: 59 - 68
