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Persistent astrocyte activation in the fragile X mouse cerebellum
BACKGROUND: Fragile X Syndrome, the most common single gene cause of autism, results from loss of the RNA‐binding protein FMRP. Although FMRP is highly expressed in neurons, it has also recently been identified in glia. It has been postulated that in the absence of FMRP, abnormal function of non‐neu...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614053/ https://www.ncbi.nlm.nih.gov/pubmed/26516618 http://dx.doi.org/10.1002/brb3.400 |