Correlation Between Vanishing White Matter Disease and Novel Heterozygous EIF2B3 Variants Using Next-Generation Sequencing: A Case Report
Sung Eun Hyun, Byung Se Choi, Ja-Hyun Jang, Inpyo Jeon, Dae-Hyun Jang, Ju Seok Ryu
Ann Rehabil Med. 2019;43(2):234-238.   Published online 2019 Apr 30     DOI: https://doi.org/10.5535/arm.2019.43.2.234
Citations to this article as recorded by Crossref logo
A (dis)integrated stress response: Genetic diseases of eIF2α regulators
Alyssa M. English, Katelyn M. Green, Stephanie L. Moon
WIREs RNA.2022;[Epub]     CrossRef
Adult Onset Vanishing White Matter Disease: A Rare Case Report
Govind Nagdev, Rajeshwari S Vhora, Gajanan Chavan, Gaurav Sahu
Cureus.2022;[Epub]     CrossRef
Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish
Yu-Ri Lee, Se Hee Kim, Afif Ben-Mahmoud, Oc-Hee Kim, Tae-Ik Choi, Kang-Han Lee, Bonsu Ku, Juneyong Eum, Yun Kee, Sangkyu Lee, Jihoon Cha, DongJu Won, Seung-Tae Lee, Jong Rak Choi, Joon Soo Lee, Heung Dong Kim, Hyung-Goo Kim, Joshua L Bonkowsky, Hoon-Chul
Human Molecular Genetics.2021; 30(5): 331.     CrossRef
Profile of Indian Children with Childhood Ataxia and Central Nervous System Hypomyelination/Vanishing White Matter Disease: A Single Center Experience from Southern India
Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, Balamurugan Nagarajan, Maya Bhat, Sanjay K. Shivappa, Naveen Benakappa
Journal of Pediatric Genetics.2021; 10(03): 205.     CrossRef