EIF2B5 mutations compromise GFAP+ astrocyte generation in vanishing white matter leukodystrophy-Reference-Cited by-同舟云学术

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EIF2B5 mutations compromise GFAP+ astrocyte generation in vanishing white matter leukodystrophy

Published:2005-02-20 Issue:3 Volume:11 Page:277-283
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Dietrich Jörg,Lacagnina Michelle,Gass David,Richfield Eric,Mayer-Pröschel Margot,Noble Mark,Torres Carlos,Pröschel Christoph

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm1195.pdf

Reference47 articles.

1. van der Knaap, M.S. et al. A new leukoencephalopathy with vanishing white matter. Neurology 48, 845–855 (1997).

2. Schiffmann, R. et al. Childhood ataxia with diffuse central nervous system hypomyelination. Ann. Neurol. 35, 331–340 (1994).

3. Hanefeld, F. et al. Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopy. Neuropediatrics 24, 244–248 (1993).

4. Fogli, A. et al. Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus. Ann. Neurol. 52, 506–510 (2002).

5. Fogli, A. et al. A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation. Neurology 59, 1966–1968 (2002).

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