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Enhancement of postsynaptic GABA(A) and extrasynaptic NMDA receptor-mediated responses in the barrel cortex of Mecp2-null mice
Rett syndrome (RTT) is a neurodevelopmental disorder that results from mutations in the X-linked gene for methyl-CpG-binding protein 2 (MECP2). The underlying cellular mechanism for the sensory deficits in patients with RTT is largely unknown. This study used the Bird mouse model of RTT to investiga...
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| Publicat a: | J Neurophysiol |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Physiological Society
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4808090/ https://ncbi.nlm.nih.gov/pubmed/26683074 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/jn.00944.2015 |
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