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

Leanne M. Dibbens*, Saul Mullen, Ingo Helbig, Heather C. Mefford, Marta A. Bayly, Susannah Bellows, Costin Leu, Holger Trucks, Tanja Obermeier, Michael Wittig, Andre Franke, Hande Caglayan, Zuhal Yapici, Thomas Sander, Evan E. Eichler, Ingrid E. Scheffer, John C. Mulley, Samuel F. Berkovic, P. De Jonghe, A. SulsH. Hjalgrim, J. M. Madsen, R. S. Møller, A. E. Lehesjoki, A. Siren, V. Gaus, D. Janz, B. Schmitz, C. E. Elger, K. Hallmann, A. A. Kleefuß-Lie, W. S. Kunz, A. Raabe, H. Muhle, P. Ostertag, S. von Spiczak, U. Stephani, H. Lerche, Y. G. Weber, P. Striano, F. Zara, C. Marini, E. H. Brilstra, D. Kastelijn-Nolst Trenité, B. P.C. Koeleman, C. G.F. de Kovel, D. Lindhout, M. E.M. Swinkels, O. Yalcin, B. Baykan, D. Turkdogan, G. Dizdarer, C. Ozkara, Y. Lee, J. Müller-Quernheim, R. Fölster-Holst, S. Hofmann, A. Nebel, T. H. Karlsen, M. Schürmann, E. Rodriguez, S. Weidinger, H. Baurecht, B. A. Lie, K. M. Boberg, T. H. Karlsen

*Corresponding author for this work
164 Citations (Scopus)

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