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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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| Publicat a: | Nature |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2021
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| Matèries: | |
| Accés en línia: | 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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