Now showing items 1-2 of 2

    • Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. 

      Møller, RS; Weber, YG; Klitten, LL; Trucks, H; Muhle, H; Kunz, WS; Mefford, HC; Franke, A; Kautza, M; Wolf, P; Dennig, D; Schreiber, S; Rückert, IM; Wichmann, HE; Ernst, JP; Schurmann, C; Grabe, HJ; Tommerup, N; Stephani, U; Lerche, H; Hjalgrim, H; Helbig, I; Sander, T; EPICURE, Consortium. (2013-02-01)
    • Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. 

      EPICURE, Consortium.; Leu, C; de, Kovel; Zara, F; Striano, P; Pezzella, M; Robbiano, A; Bianchi, A; Bisulli, F; Coppola, A; Giallonardo, AT; Beccaria, F; Trenité, DK; Lindhout, D; Gaus, V; Schmitz, B; Janz, D; Weber, YG; Becker, F; Lerche, H; Kleefuss-Lie, AA; Hallman, K; Kunz, WS; Elger, CE; Muhle, H; Stephani, U; Møller, RS; Hjalgrim, H; Mullen, S; Scheffer, IE; Berkovic, SF; Everett, KV; Gardiner, MR; Marini, C; Guerrini, R; Lehesjoki, AE; Siren, A; Nabbout, R; Baulac, S; Leguern, E; Serratosa, JM; Rosenow, F; Feucht, M; Unterberger, I; Covanis, A; Suls, A; Weckhuysen, S; Kaneva, R; Caglayan, H; Turkdogan, D; Baykan, B; Bebek, N; Ozbek, U; Hempelmann, A; Schulz, H; Rüschendorf, F; Trucks, H; Nürnberg, P; Avanzini, G; Koeleman, BP; Sander, T (2012-02-01)