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Presymptomatic training mitigates functional deficits in Rett syndrome mice

Mutations in the X-linked gene MECP2 cause Rett syndrome, a progressive neurological disorder in which children develop normally for the first one or two years of life before experiencing profound motor and cognitive decline(1,2,3). Currently, there are no effective treatments for Rett syndrome, but...

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Detalhes bibliográficos
Publicado no:Nature
Main Authors: Achilly, Nathan P., Wang, Wei, Zoghbi, Huda Y.
Formato: Artigo
Idioma:Inglês
Publicado em: 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8093094/
https://ncbi.nlm.nih.gov/pubmed/33762729
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41586-021-03369-7
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