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...

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Detalles Bibliográficos
Autores principales: Deng, Jiong, Zhang, Jie, Gao, Kai, Zhou, Ling, Jiang, Yuwu, Wang, Jingmin, Wu, Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
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

Internet

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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