Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy-Reference-Cited by-同舟云学术

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

Published:1998-10 Issue:2 Volume:20 Page:171-174
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Minassian Berge A.,Lee Jeffrey R.,Herbrick Jo-Anne,Huizenga Jack,Soder Sylvia,Mungall Andrew J.,Dunham Ian,Gardner Rebecca,Fong Chung-yan G.,Carpenter Stirling,Jardim Laura,Satishchandra P.,Andermann Eva,Snead O. Carter,Lopes-Cendes Iscia,Tsui Lap-Chee,Delgado-Escueta Antonio V.,Rouleau Guy A.,Scherer Stephen W.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1098_171.pdf

Reference24 articles.

1. Berkovic, S.F., Andermann, F., Carpenter, S. & Wolfe, L.S. Progressive myoclonus epilepsies: specific causes and diagnosis. New Eng. J. Med. 315, 296–305 (1986).

2. Van Heycop Ten Ham, M.W. Lafora disease, a form of progressive myoclonus epilepsy. Handbook of Clinical Neurology 15, 382–422 (1974).

3. Minassian, B.A., Sainz, J., Bohlega, S., Sakamoto, L.M. & Delgado-Escueta, A.V. Genetic heterogeneity in Lafora's disease . Epilepsia 37, 126 ( 1996).

4. Lafora, G.R. Uber das vorkommen amyloider korperchen im innern der ganglienzellen; zugleich ein beitrag zum studium der amyloiden substanz im nervensystem. Virchows. Arch. Path. Anat. 205, 295– 303 (1911).

5. Harriman, D.G. & Millar, J.H.D. Progressive familial myoclonic epilepsy in 3 families: its clinical features and pathological basis. Brain 78, 325–349 ( 1955).

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