Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.

Dibbens, LM;Mullen, S;Helbig, I;Mefford, HC;Bayly, MA;Bellows S;Leu C;Trucks, H;Obermeier, T;Wittig, M;Franke, A;Caglayan, H;Yapici, Z;Sander, T;Eichler, EE;Scheffer, IE;Mulley, JC;Berkovic, SF;De Jonghe, P;Suls, A;Hjalgrim, H;Madsen, JM;Møller, RS;Lehesjoki, AE;Siren, A;Gaus, V;Janz, D;Schmitz, B;Elger, CE;Hallmann, K;Kleefuß-Lie, AA;Kunz, WS;Raabe, A;Muhle, H;Ostertag, P;von Spiczak, S;Stephani, U;Lerche, H;Weber, YG;Striano, P;Zara, F;Marini, C;Brilstra, EH;Kastelijn-Nolst Trenité;D Koeleman;BPC;de Kovel, CGF;Lindhout, D;Swinkels, MEM;Yalcin, O;Baykan, B;Turkdogan, D;Dizdarer, G;Ozkara, C;Lee, Y;Müller-Quernheim, J;Fölster-Holst, R;Hofmann, S;Nebel, A.;Schreiber, S;Schürmann, M;Rodriguez, E;Weidinger S;Baurecht H;Lie, BA;Boberg, KM;Karlsen, TH.

2009-01-01