Kyndt F.,2001
Kyndt F., Probst V., Potet F., Demolombe S., Chevallier J.C., Baro I., Moisan J.P., Boisseau P., Schott J.J., Escande D., Le Marec H. Novel SCN5A mutation leading either to isolated conduction defect or Brugada syndrome in a large French family. - Circulation, 2001, v. 104, p. 3081-3086.
