Journal
Frontiers in Genetics
Publication Date
1-1-2022
Volume
13
First Page
893057
Document Type
Open Access Publication
DOI
10.3389/fgene.2022.893057
Rights and Permissions
Wongkittichote P, Mar SS, McKinstry RC and Nguyen H (2022) Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter. Front. Genet. 13:893057. doi: 10.3389/fgene.2022.893057 © 2022 Wongkittichote, Mar, McKinstry and Nguyen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Recommended Citation
Wongkittichote, Parith; Mar, Soe Soe; McKinstry, Robert C; and Nguyen, Hoanh, "Case report: A novel EIF2B3 pathogenic variant in central nervous system hypomyelination/vanishing white matter." Frontiers in Genetics. 13, 893057 (2022).
https://digitalcommons.wustl.edu/oa_4/125
