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Early differential impact of MeCP2 mutations on functional networks in Rett syndrome patient-derived human cortical organoids

Abstract Human cerebral organoids derived from induced pluripotent stem cells can recapture early developmental processes and reveal changes involving neurodevelopmental disorders. Mutations in the X-linked methyl-CpG binding protein 2 (MECP2) gene are associated with Rett syndrome, and disease seve...

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Egile Nagusiak: Tatsuya Osaki, Chloe Delepine, Yuma Osako, Devorah Kranz, April Levin, Charles Nelson, Michela Fagiolini, Mriganka Sur
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Nature Portfolio 2026-04-01
Saila:Nature Communications
Sarrera elektronikoa:https://doi.org/10.1038/s41467-026-71458-0
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