Mutations of DEPDC5 cause autosomal dominant focal epilepsies-Reference-Cited by-同舟云学术

Mutations of DEPDC5 cause autosomal dominant focal epilepsies

Published:2013-03-31 Issue:5 Volume:45 Page:552-555
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ishida Saeko,Picard Fabienne,Rudolf Gabrielle,Noé Eric,Achaz Guillaume,Thomas Pierre,Genton Pierre,Mundwiller Emeline,Wolff Markus,Marescaux Christian,Miles Richard,Baulac Michel,Hirsch Edouard,Leguern Eric,Baulac Stéphanie

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2601.pdf

Reference18 articles.

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2. Berkovic, S.F. et al. Familial temporal lobe epilepsy: a common disorder identified in twins. Ann. Neurol. 40, 227–235 (1996).

3. Ottman, R. et al. Localization of a gene for partial epilepsy to chromosome 10q. Nat. Genet. 10, 56–60 (1995).

4. Klein, K.M. et al. Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum. Epilepsia 53, e151–e155 (2012).

5. Baulac, S. & Baulac, M. Advances on the genetics of mendelian idiopathic epilepsies. Clin. Lab. Med. 30, 911–929 (2010).

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