1Chen Q, Kitsch GE, Zhang D, et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature. 1998;392:293 - 296.
2Bezzina C, Veldkamp MW, Van den Berg MP, et al. A single Nachannel mutation causing both long - QT and Brugada syndromes. Circ Res. 1999 ; 85:1206 - 1213.
3Priori SG, Napolitano C, Gasparini Met al. Natural history of Brugada syndrome: insights for risk stratification and management. Circulation. 2002; 105 : 1342 - 1347.
4Kyndt F, Probst V, Potet F et al. Novel SCNSA mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family Circulation. 2001 ; 104 : 3081 - 3086.