Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders-Reference-Cited by-同舟云学术

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

Published:2013-01-20 Issue:1 Volume:14 Page:23-34
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

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

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-013-0353-1.pdf

Reference32 articles.

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