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Human‐induced pluripotent stem cell‐derived cerebral organoid of leukoencephalopathy with vanishing white matter
INTRODUCTION: Leukoencephalopathy with vanishing white matter (VWM) is a rare autosomal recessive leukoencephalopathy resulting from mutations in EIF2B1‐5, which encode subunits of eukaryotic translation initiation factor 2B (eIF2B). Studies have found that eIF2B mutation has a certain influence on...
Autores principales: | Deng, Jiong, Zhang, Jie, Gao, Kai, Zhou, Ling, Jiang, Yuwu, Wang, Jingmin, Wu, Ye |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018084/ https://www.ncbi.nlm.nih.gov/pubmed/36650674 http://dx.doi.org/10.1111/cns.14079 |
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