Lack of SCN1A mutations in familial febrile seizures

Malacarne M., Madia F., Gennaro E., Vacca D., Guney I., Buono S., ...Daha Fazla

EPILEPSIA, cilt.43, ss.559-562, 2002 (SCI İndekslerine Giren Dergi) identifier identifier identifier


Purpose: Mutations in the voltage-gated sodium channel subunit gene SCN1A have been associated with febrile seizures (FSs) in autosomal dominant generalized epilepsy with febrile seizures plus (GEFS(+)) families and severe myoclonic epilepsy of infancy. The present study assessed the role of SCN1A in familial typical FSs.