1. Lee, Yu-Ri, Kim, Se Hee, Ben-Mahmoud, Afif, Kang, Hoon-Chul, Kim, Cheol-Hee. . Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish. In Human molecular genetics, 30, 331-342. doi:10.1093/hmg/ddab033. https://pubmed.ncbi.nlm.nih.gov/33517449/
2. Kim, Doeun, Lee, Yu-Ri, Choi, Tae-Ik, Kim, Cheol-Hee, Lee, Sangkyu. 2021. Comparative Proteome Research in a Zebrafish Model for Vanishing White Matter Disease. In International journal of molecular sciences, 22, . doi:10.3390/ijms22052707. https://pubmed.ncbi.nlm.nih.gov/33800130/
3. Chen, Na, Dai, Lifang, Jiang, Yuwu, Zang, Lili, Wu, Ye. 2015. Endoplasmic reticulum stress intolerance in EIF2B3 mutant oligodendrocytes is modulated by depressed autophagy. In Brain & development, 38, 507-15. doi:10.1016/j.braindev.2015.11.002. https://pubmed.ncbi.nlm.nih.gov/26625702/
4. Wongkittichote, Parith, Mar, Soe Soe, McKinstry, Robert C, Nguyen, Hoanh. 2022. Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter. In Frontiers in genetics, 13, 893057. doi:10.3389/fgene.2022.893057. https://pubmed.ncbi.nlm.nih.gov/35783294/
5. La Piana, Roberta, Vanderver, Adeline, van der Knaap, Marjo, Brais, Bernard, Bernard, Geneviève. . Adult-onset vanishing white matter disease due to a novel EIF2B3 mutation. In Archives of neurology, 69, 765-68. doi:10.1001/archneurol.2011.1942. https://pubmed.ncbi.nlm.nih.gov/22312164/
6. Thuppanattumadam Ananthasubramanian, Sangeeth, Arunachal, Gautham, Padmanabha, Hansashree, Mahale, Rohan Ramachandra. 2024. Adult-Onset EIF2B-Pathies: A Clinical, Imaging and Genetic Profiling with Literature Review. In The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, , 1-8. doi:10.1017/cjn.2024.308. https://pubmed.ncbi.nlm.nih.gov/39450483/
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