Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features-Reference-Cited by-同舟云学术

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

Published:2002-01-28 Issue:3 Volume:30 Page:335-341
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Kalachikov Sergey,Evgrafov Oleg,Ross Barbara,Winawer Melodie,Barker-Cummings Christie,Boneschi Filippo Martinelli,Choi Chang,Morozov Pavel,Das Kamna,Teplitskaya Elita,Yu Andrew,Cayanis Eftihia,Penchaszadeh Graciela,Kottmann Andreas H.,Pedley Timothy A.,Hauser W. Allen,Ottman Ruth,Gilliam T. Conrad

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng832z.pdf

Reference30 articles.

1. Hauser, W.A., Annegers, J.F. & Kurland, L.T. Prevalence of epilepsy in Rochester, Minnesota: 1940–1980. Epilepsia 32, 429–445 (1991).

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

3. Winawer, M.R., Ottman, R., Hauser, W.A. & Pedley, T.A. Autosomal dominant partial epilepsy with auditory features: defining the phenotype. Neurology 54, 2173–2176 (2000).

4. Poza, J.J. et al. Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. Ann. Neurol. 45, 182–188 (1999).

5. Michelucci, R. et al. Autosomal dominant partial epilepsy with auditory features: description of a new family. Epilepsia 41, 967–970 (2000).

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