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Structural and functional differences in the barrel cortex of Mecp2 null mice
Functional deficits in sensory systems are commonly noted in neurodevelopmental disorders, such as the Rett syndrome (RTT). Defects in methyl CpG binding protein gene (MECP2) largely accounts for RTT. Manipulations of the Mecp2 gene in mice provide useful models to probe into various aspects of brai...
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| Publicado no: | J Comp Neurol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5994756/ https://ncbi.nlm.nih.gov/pubmed/28857161 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cne.24315 |
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