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, sa.5, ss.559-62, 2002 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 43 Konu: 5
  • Basım Tarihi: 2002
  • Doi Numarası: 10.1046/j.1528-1157.2002.29301.x
  • Dergi Adı: Epilepsia
  • Sayfa Sayıları: ss.559-62

Özet

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.