The latest on leukodystrophies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference27 articles.
1. An update on the leukodsytrophies
2. Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter
3. Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter
4. Leukoencephalopathy With Vanishing White Matter: From Magnetic Resonance Imaging Pattern to Five Genes
5. Regulation of mammalian translation factors by nutrients
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2. Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease;Frontiers in Pediatrics;2022-05-24
3. White matter and neurological disorders;Archives of Pharmacal Research;2020-09
4. Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during Infancy;The American Journal of Human Genetics;2019-11
5. Heterozygous variants in the mechanosensitive ion channelTMEM63Aresult in transient hypomyelination during infancy;2019-07-03
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