Pippo K.,2001
Pippo K., Swan H., Pasternack M., Chapman H., Paavonen K., Viitasalo M., Toivonen L., Kontuka K. A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics. - J.Am.Coll.Cardiol., 2001, v. 37, p. 562-568.
Смотрите также:
