Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy-Reference-Cited by-同舟云学术

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

Published:2002-03-11 Issue:4 Volume:30 Page:441-445
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Strømme Petter,Mangelsdorf Marie E.,Shaw Marie A.,Lower Karen M.,Lewis Suzanne M.E.,Bruyere Helene,Lütcherath Viggo,Gedeon Ági K.,Wallace Robyn H.,Scheffer Ingrid E.,Turner Gillian,Partington Michael,Frints Suzanna G.M.,Fryns Jean-Pierre,Sutherland Grant R.,Mulley John C.,Gécz Jozef

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng862z.pdf

Reference29 articles.

1. Chelly, J. & Mandel, J.L. Monogenic causes of X-linked mental retardation. Nature Rev. Genet. 2, 669–680 (2001).

2. Berkovic, S.F. & Scheffer, I.E. Genetics of the epilepsies. Epilepsia 42 (Suppl. 5), 16–23 (2001).

3. Brais, B. et al. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nature Genet. 18, 164–167 (1998).

4. Gusella, J.F. & MacDonald, M.E. Molecular genetics: unmasking polyglutamine triggers in neurodegenerative disease. Nature Rev. Neurosci. 1, 109–115 (2000).

5. Wong, M. & Trevathan, E. Infantile spasms. Pediatr. Neurol. 24, 89–98 (2001).

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