Neyroud N.,1998


Neyroud N., Denjoy I., Donger C., Gary F., Villain E., Leenhardt A., Benali K., Schwartz K., Coumel P., Guicheney P. Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome. - Eur.J.Hum.Genet., 1998, v. 6, p. 129-133.

Смотрите также:

  • Синдром LQT1