共 50 条
- [25] EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report Italian Journal of Pediatrics, 48
- [28] A RARE MUTATION IN EIF2B4 GENE IN AN EPILEPTIC CHILD WITH VANISHING WHITE MATTER DISEASE: A CASE REPORT GENETIC COUNSELING, 2015, 26 (01): : 41 - 46
- [29] The Arg113His mutation of the translation initiation factor (eIF2B5) associated with the adult onset of vanishing white matter is not present in multiple sclerosis MULTIPLE SCLEROSIS, 2005, 11 : S116 - S116