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