Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation

Autor: Blumkin, Lubov, Suls, Arvid, Deconinck, Tine, De Jonghe, Peter, Linder, Ilan, Kivity, Sara, Dabby, Ron, Leshinsky-Silver, Esther, Lev, Dorit, Lerman-Sagie, Tally
Zdroj: In European Journal of Paediatric Neurology July 2012 16(4):356-360
Databáze: ScienceDirect