Appenzeller, SilkeBalling, RudiBarisic, NinaBaulac, StephanieCaglayan, HandeCraiu, DanaDe Jonghe, PeterDepienne, ChristelDimova, PetiaDjemie, TaniaGormley, PadhraigGuerrini, RenzoHelbig, IngoHjalgrim, HelleHoffman-Zacharska, DorotaJaehn, JohannaKlein, Karl MartinKoeleman, BobbyKomarek, VladimirKrause, RolandKuhlenbaeumer, GregorLeguern, EricLehesjoki, Anna-ElinaLemke, Johannes R.Lerche, HolgerLinnankivi, TarjaMarini, CarlaMay, PatrickMoller, Rikke S.Muhle, HiltrudPal, DebPalotie, AarnoPendziwiat, ManuelaRobbiano, AngelaRoelens, FilipRosenow, FelixSelmer, KajaSerratosa, Jose M.Sisodiya, SanjayStephani, UlrichSterbova, KatalinStriano, PasqualeSuls, ArvidTalvik, Tiinavon Spiczak, SarahWeber, YvonneWeckhuysen, SarahZara, FedericoAbou-Khalil, BasselAlldredge, Brian K.EuroEPINOMICS-RES ConsortiumEpilepsy Phenome Genome ProjectEpi4K Consortium2018-01-292018-01-292014-10-02Appenzeller, S, Balling, R, Barisic, N, Baulac, S, Caglayan, H, Craiu, D, De Jonghe, P, Depienne, C, Dimova, P, Djemie, T, Gormley, P, Guerrini, R, Helbig, I, Hjalgrim, H, Hoffman-Zacharska, D, Jaehn, J, Klein, K M, Koeleman, B, Komarek, V, Krause, R, Kuhlenbaeumer, G, Leguern, E, Lehesjoki, A-E, Lemke, J R, Lerche, H, Linnankivi, T, Marini, C, May, P, Moller, R S, Muhle, H, Pal, D, Palotie, A, Pendziwiat, M, Robbiano, A, Roelens, F, Rosenow, F, Selmer, K, Serratosa, J M, Sisodiya, S, Stephani, U, Sterbova, K, Striano, P, Suls, A, Talvik, T, von Spiczak, S, Weber, Y, Weckhuysen, S, Zara, F, Abou-Khalil, B, Alldredge, B K, EuroEPINOMICS-RES Consortium, Epilepsy Phenome Genome Project & Epi4K Consortium 2014, 'De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies', American Journal of Human Genetics, vol. 95, no. 4, pp. 360-370. https://doi.org/10.1016/j.ajhg.2014.08.013ORCID: /0000-0002-2527-5874/work/97266246http://hdl.handle.net/10138/23172511enginfo:eu-repo/semantics/openAccessINTELLECTUAL DISABILITYSPECTRUM DISORDERSGRIN2A MUTATIONSSCHIZOPHRENIAEPILEPSIESAUTISMENDOCYTOSISDYNAMIN-1PATTERNSAPHASIANeurosciencesDe Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic EncephalopathiesArticleopenAccesse263e9a5-2b00-4e1f-b92c-525f3d67131384921803785000342654300002