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Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome–like phenotypes
Mutations in the X-linked gene encoding methyl-CpG–binding protein 2 (MeCP2) cause Rett syndrome (RTT), a neurological disorder affecting cognitive development, respiration, and motor function. Genetic restoration of MeCP2 expression reverses RTT-like phenotypes in mice, highlighting the need to sea...
Guardat en:
| Publicat a: | J Clin Invest |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5409785/ https://ncbi.nlm.nih.gov/pubmed/28394263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI90967 |
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