EIF2B4 gene

Known as: EIF2B4, EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, DELTA, EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, SUBUNIT 4 
This gene is involved in both the initiation and regulation of protein synthesis.
National Institutes of Health

Papers overview

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2018
2018
Leukoencephalopathy with vanishing white matter (VWM; MIM #603896) is an autosomal recessive disorder, characterized by childhood… (More)
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2015
2015
To the Editor: Vanishing white matter disease (VWM) is one of the most prevalent inherited leucoencephalopathies with autosomal… (More)
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2008
2008
The critical role of protein synthesis in regulating lifespan has been evidenced. This study shows that adult-onset RNAi… (More)
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2007
2007
“ Vanishing white matter ” (VWM) or “ childhood ataxia with central hypomyelination ” (CACH) is an autosomal recessive disorder… (More)
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Review
2006
Review
2006
Vanishing white matter disease (VWM; MIM #603896), also known as childhood ataxia with central nervous system hypomyelination… (More)
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Chronic fatigue syndrome (CFS) is a multisystem disease, the pathogenesis of which remains undetermined. AIMS To… (More)
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2005
2005
Autosomal recessive inherited mutations in each of the five eukaryotic initiation factor 2B (eIF2B) subunits are known to cause… (More)
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Highly Cited
2004
Highly Cited
2004
Childhood ataxia with central nervous system hypomyelination (CACH), or vanishing white matter leukoencephalopathy (VWM), is a… (More)
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Review
2003
Review
2003
Leukoencephalopathy with vanishing white matter can be diagnosed on the basis of distinct clinical and magnetic resonance imaging… (More)
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