Neyroud N.,1997


Neyroud N., Tesson F., Denjoy I., Leibovici M., Donger C., Barhanin J., Faure S., Gary F., Coumel P., Petit C., Schwartz K., Guicheney P. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lang-Nielsen cardioaudtory syndrome. - Nature Genet., 1997, v. 15, p. 186-189.

Смотрите также:

  • Синдром LQT1