Case report: A novel EIF2B3 pathogenic variant in central nervous system hypomyelination/vanishing white matter

Authors

Parith Wongkittichote, Washington University School of Medicine in St. Louis
Soe Soe Mar, Washington University School of Medicine in St. Louis
Robert C McKinstry, Washington University School of Medicine in St. Louis
Hoanh Nguyen, Washington University School of Medicine in St. Louis

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