Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter-Reference-Cited by-同舟云学术

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Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter

Published:2001-12-27 Issue:2 Volume:51 Page:264-270
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

van der Knaap Marjo S.,Leegwater Peter A. J.,Könst Andrea A.M.,Visser Allerdien,Naidu Sakkubai,Oudejans Cees B.M.,Schutgens Ruud B.H.,Pronk Jan C.

Funder

Dutch Organisation for Scientific Research, NWO

Dr. W.M. Phelps Foundation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference27 articles.

1. Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach;Van der Knaap;Radiology,1999

2. Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopy;Hanefeld;Neuropediatrics,1993

3. A new leukoencephalopathy with vanishing white matter;van der Knaap;Neurology,1997

4. Childhood ataxia with diffuse central nervous system hypomyelination;Schiffmann;Ann Neurol,1994

5. Fatal infantile leukodystrophy, a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27;Francalanci;Neurology,2001

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