TY - JOUR AU - Suls, A; Jaehn, J A; Kecskés, A TI - De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome JO - Am J Hum Genet IS - 5 VL - 93 PY - 2013 DO - 10.1016/j.ajhg.2013.09.017 SP - 967 EP - 975 N1 - , et al; EuroEPINOMICS RES Consortium. ER -