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Wild type microglia arrest pathology in a mouse model of Rett syndrome
Rett syndrome is an X-linked autism spectrum disorder. The disease is characterized in the majority of cases by mutation of the MECP2 gene, which encodes a methyl-CpG-binding protein (1–5). Although MeCP2 is expressed in many tissues, the disease is generally attributed to a primary neuronal dysfunc...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3321067/ https://ncbi.nlm.nih.gov/pubmed/22425995 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature10907 |
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