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Dibbens, L.M., Mullen, S., Helbig, I., Mefford, H.C., Bayly, M.A., Bellows, S., Leu, C., Trucks, H., Obermeier, T., Wittig, M., Franke, A., Caglayan, H., Yapici, Z., EPICURE Consortium, Sander, T., Eichler, E.E., Scheffer, I.E., Mulley, J.C. and Berkovic, S.F. (2009) Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: Precedent for disorders with complex inheritance. Human Molecular Genetics, 18, 3626-3631. doi:10.1093/hmg/ddp311

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