Published 2013 | Version v1

Publication Metadata-only

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

Creators: 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

Others:: 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

Additional details

Created:: April 14, 2023
Modified:: November 23, 2023