Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death.

Partemi S;Cestèle S;Pezzella M;Campuzano O;Paravidino R;Pascali VL;Zara F;Tassinari CA;Striano S;Oliva A;Brugada R;Mantegazza M;STRIANO, PASQUALE

2013-01-01