Suls, A., Jaehn, J., Kecskes, A., Weber, Y., Weckhuysen, S., Craiu, D., Siekierska, A., Djemie, T., Afrikanova, T., Gormley, P., von Spiczak, S., Kluger, G., Iliescu, C., Talvik, T., Talvik, I., Meral, C., Caglayan, H., Giraldez, B., Serratosa, J.,...Lemke, J. (2013) De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS , 93(5), 967-975.