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Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout rats
BACKGROUND: Rett Syndrome (RTT) is a neurodevelopmental disease caused by the disruption of the MECP2 gene. Several mouse models of RTT have been developed with Mecp2 disruptions. Although the mouse models are widely used in RTT research, results obtained need to be validated in other species. There...
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| Publicado no: | J Neurodev Disord |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4910223/ https://ncbi.nlm.nih.gov/pubmed/27313794 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-016-9156-7 |
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