1.
Yalçın Ö, Çağlayan SH, Saltık S, et al. A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC). Turk J Pediatr. 2007;49(4):385-389. doi:10.24953/turkjpediatr.2007.2571