Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease (2022)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-022-01050-9
PubMed Identifier: 35217805
Publication URI: http://europepmc.org/abstract/MED/35217805
Type: Journal Article/Review
Parent Publication: European Journal of Human Genetics
Issue: 7
ISSN: 1018-4813