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EIF2B1 gene

Known as: EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, SUBUNIT 1, eukaryotic translation initiation factor 2B subunit alpha, EIF2B-ALPHA 
This gene is involved in the initiation of protein synthesis.
National Institutes of Health

Related topics

Related topics

11 relations
EIF2B1 protein, humanEIF2B3 geneEIF2B4 geneEIF2B4 protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Fifteen Novel EIF2B1-5 Mutations Identified in Chinese Children with Leukoencephalopathy with Vanishing White Matter and a Long Term Follow-Up
Leukoencephalopathy with vanishing white matter (VWM) is one of the most prevalent inherited childhood white matter disorders… 
2013
2013
Vanishing White Matter With Hepatomegaly and Hypertriglyceridemia Attacks
Vanishing white matter disease is one of the most prevalent leukodystrophies in childhood. It is caused by mutations in any of… 
2008
2008
No evidence that polymorphisms of the vanishing white matter disease genes are risk factors in multiple sclerosis
Febrile infections are known to cause exacerbations in the white matter disorders ‘vanishing white matter’ (VWM) and multiple… 
2005
2005
Vanishing white matter disease in a child presenting with ataxia
Abstract:  Vanishing white matter disease is a recently described leukoencephalopathy that is characterized by chronic and… 
2002
2002
[From gene to disease; a defect in the regulation of protein production leading to vanishing white matter].
Leukoencephalopathy with vanishing white matter (VWM) is a newly defined autosomal recessive disorder. The clinical course is… 
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