Lack of SCN1A mutations in familial febrile seizures.

Malacarne, M; Madia, F; Gennaro, E; Vacca, D; Guney, AHMET; Buono, S; Dalla Bernardina, B; Gaggero, R; Gobbi, G; Lispi, ML; Malamaci, D; Melideo, G; Roccella, M; Sferro, C; Tiberti, A; Vanadia, F; Vigevano, F; Viri, F; Vitali, MR; Bricarelli, FD; Bianchi, A; Zara, F

doi:10.1046/j.1528-1157.2002.29301.x

Lack of SCN1A mutations in familial febrile seizures.

Atıf İçin Kopyala

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)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 43 Sayı: 5
Basım Tarihi: 2002
Doi Numarası: 10.1046/j.1528-1157.2002.29301.x
Dergi Adı: Epilepsia
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.559-62
Marmara Üniversitesi Adresli: Evet

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.