Sign Up to like & get
recommendations!
0
Published in 2021 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2021.729777
Abstract: 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…
read more here.
Keywords:
age;
correlation genotype;
age onset;
genotype age ... See more keywords