Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter

MLA

Parith Wongkittichote, et al. “Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter.” Frontiers in Genetics, vol. 13, June 2022. EBSCOhost, https://doi.org/10.3389/fgene.2022.893057.

APA

Parith Wongkittichote, Soe Soe Mar, Robert C. McKinstry, & Hoanh Nguyen. (2022). Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.893057

Chicago

Parith Wongkittichote, Soe Soe Mar, Robert C. McKinstry, and Hoanh Nguyen. 2022. “Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter.” Frontiers in Genetics 13 (June). doi:10.3389/fgene.2022.893057.