Diagnostic implications of genetic copy number variation in epilepsy plus
- Resource Type
- Authors
- Coppola, A1; 2, 3; Cellini, E4; Stamberger, H5; 6, 7; Saarentaus, E8; 9, 10; Cetica, V4; Lal, D10; 11, 12; Djémié, T5; 6; Bartnik-Glaska, M13; Ceulemans, B14; Cross, JH15; 16, 17; Deconinck, T5; De Masi S7; Dorn, T18; Guerrini, R; Hoffman-Zacharska, D14; Kooy, F19; Lagae, L20; Lench, N21; Lemke, JR22; Lucenteforte, E23; Madia, F25; Mefford, HC26; Morrogh, D21; Nuernberg, P27; Palotie, A11; Schoonjans, AS15; Striano, P28; Szczepanik, E29; Tostevin, A1; 2; Vermeesch, JR30; Van Esch H30; Van Paesschen W31; Waters, JJ21; Weckhuysen, S5; 6, 12; Zara, F25; De Jonghe P5; Sisodiya, SM1; Marini, C; EuroEPINOMICS-RES, Consortium; Lehesjioki AE, EpiCNV Consortium.; Craiu, D; Talvik, T; Caglayan, H; Serratosa, J; Sterbova, K; Møller, Rs; Hjalgrim, H; Lerche, H; Weber, Y; Helbig, I; von Spiczak, S; Barba, C; Bogaerts, A; Boni, A; Galizia, Ec; Chiari, S; Di Gacomo, G; Ferrari, A; Garducci, S; Giglio, S; Holmgren, P; Leu, C; Melani, F; Novara, F; Pantaleo, M; Peeters, E; Pisano, T; Rosati, A; Sander, J; Schoeler, N; Stankiewicz, P; Striano, S; Suls, A; Traverso, M; Vandeweyer, G; Van Dijck, A; Zuffardi, O.
- Source
- Subject
- epilepsy
- Language
- English