Correlation Between Genotype and Age of Onset in Leukoencephalopathy With Vanishing White Matter

Purpose: Leukoencephalopathy with vanishing white matter (VWM) is an autosomal recessive leukoencephalopathy caused by mutations in any of the five genes encoding the subunits of eukaryotic translation initiation factor 2B (eIF2B). The severity of the disease varies considerably, and its genotypic-p...

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Bibliographic Details
Main Authors: Jiong Deng, Ling Zhou, Jie Zhang, Xuting Chang, Yuwu Jiang, Jingmin Wang, Ye Wu
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-10-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.729777/full