Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleClinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.AuthorsHarssel, J.; Weckhuysen, S.; Kempen, M.; Hardies, K.; Verbeek, N.; Kovel, C.; Gunning, W.; Daalen, E.; Jonge, M.; Jansen, A.; Vermeulen, R.; Arts, W.; Verhelst, H.; Fogarasi, A.; Rijk-van Andel, J.; Kelemen, A.; Lindhout, D.; Jonghe, P.; Koeleman, B.; Suls, A.PublicationNeurogenetics, 2013, Vol 14, Issue 1, p23ISSN1364-6745Publication typeArticleDOI10.1007/s10048-013-0353-1