Genetic screening of EIF2B genes reveals mutation spectrum and predicted prevalence of vanishing white matter disease in Chinese population

Clinica Chimica Acta 2026

View at publisher

Authors: Xiaoli Liu, Ruolan Guo, Zhan Qi, Yaodong Zhang, Xiaotun Ren, Wei Li, Xuyun Hu, Chanjuan Hao

DOI: 10.1016/j.cca.2026.120942

Cited by: 0

References: 23

Fields of Study & Subjects

Metabolism and Genetic Disorders Genomics and Rare Diseases Hereditary Neurological Disorders

References 23