Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy-Reference-Cited by-同舟云学术

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

Published:2002-05-06 Issue:2 Volume:31 Page:184-189
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Cossette Patrick,Liu Lidong,Brisebois Katéri,Dong Haiheng,Lortie Anne,Vanasse Michel,Saint-Hilaire Jean-Marc,Carmant Lionel,Verner Andrei,Lu Wei-Yang,Tian Wang Yu,Rouleau Guy A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng885z.pdf

Reference30 articles.

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3. Scheffer, I.E. & Berkovic, S.F. Generalized epilepsy with febrile seizures plus: a genetic disorder with heterogeneous clinical phenotypes. Brain 120, 479–490 (1997).

4. Wallace, R.H. et al. Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel β1 subunit gene SCN1B. Nature Genet. 19, 366–370 (1998).

5. Escayg, A. et al. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nature Genet. 24, 343–345 (2000).

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