Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

J.J.T. van Harssel, S. Weckhuysen, M.J.A. van Kempen, K. Hardies, N.E. Verbeek, C.G.F. de Kovel, W.B. Gunning, E. van Daalen, M.V. de Jonge, A.C. Jansen, R.J. Vermeulen, W.F.M. Arts, H. Verhelst, A. Fogarasi, J. de Rijk-van Andel, A. Kelemen, D. Lindhout, P. De Jonghe, B.P.C. Koeleman, A. SulsE.H. Brilstra

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)23-34
Issue number1
Publication statusPublished - 2013

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