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
JournalNeurogenetics
Volume14
Issue number1
DOIs
Publication statusPublished - 2013

Cite this

van Harssel, J. J. T., Weckhuysen, S., van Kempen, M. J. A., Hardies, K., Verbeek, N. E., de Kovel, C. G. F., ... Brilstra, E. H. (2013). Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders. Neurogenetics, 14(1), 23-34. https://doi.org/10.1007/s10048-013-0353-1