Benign familial infantile convulsions: Linkage to chromosome 16p12-q12 in 14 families

Tarih
2004
Yazar
Hikel, C
Weber, YG
Berger, A
Maier, S
Karafyllakes, S
Meyer, N
Fukuyama, Y
Halbach, A
Kurlemann, G
Neubauer, B
Osawa, M
Pust, B
Rating, D
Saito, K
Stephani, U
Tauer, U
Lehmann-Horn, F
Jurkat-Rott, K
Lerche, H
Bebek, Nerses
Üst veri
Tüm öğe kaydını göster
Özet
Purpose: Benign familial infantile convulsions (BFIC) is a form of idiopathic epilepsy. It is characterized by clusters of afebrile seizures occurring around the sixth month of life. The disease has a benign course with a normal development and rare seizures in adulthood. Previous linkage analyses defined three susceptibility loci on chromosomes 19q12-q13.11, 16p12-q12, and 2q23-31. However, a responsible gene has not been identified. We studied linkage in 16 further BFIC families.
Bağlantı
http://hdl.handle.net/20.500.12627/88264
https://doi.org/10.1111/j.0013-9580.2004.48203.x
Koleksiyonlar