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EIF2B3 gene

Known as: eukaryotic translation initiation factor 2B subunit gamma, EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, GAMMA, EIF2B3 
National Institutes of Health

Related topics

Related topics

10 relations
EIF1 geneEIF1AY geneEIF2B1 geneEIF2B1 protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
[Clinical features of 54 cases of leukoencephalopathy with vanishing white matter disease in children].
  • L. ZhouH. Zhang Y. Wu
  • Zhonghua er ke za zhi = Chinese journal of…
  • 2019
  • Corpus ID: 204968753
Objective: To summarize the clinical features of leukoencephalopathy with vanishing white matter disease (VWM) in children… 
2016
2016
Endoplasmic reticulum stress intolerance in EIF2B3 mutant oligodendrocytes is modulated by depressed autophagy
2015
2015
Adult-onset vanishing white matter disease as differential diagnosis of primary progressive multiple sclerosis: A case report
We report the case of a 42-year-old woman with a slowly progressive cerebellar syndrome. In contrast to a relatively mild… 
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… 
2012
2012
Childhood Ataxia with Cerebral Hypomyelination Syndrome: A Variant of Patient with Early Childhood Onset Related to EIF2B3 Mutation
Childhood ataxia with central nervous system hypomyelination (CACH) syndrome is an autosomal recessive transmitted leukodystrophy… 
2009
2009
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease
Vanishing white matter (VWM) disease, inherited in an autosomal recessive manner, is one of the most prevalent inherited… 
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