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Dysregulation of fragile X mental retardation protein and metabotropic glutamate receptor 5 in superior frontal cortex of individuals with autism: a postmortem brain study
BACKGROUND: Fragile X syndrome is caused by loss of function of the fragile X mental retardation 1 (FMR1) gene and shares multiple phenotypes with autism. We have previously found reduced expression of the protein product of FMR1 (FMRP) in vermis of adults with autism. METHODS: In the current study,...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2011
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3488976/ https://ncbi.nlm.nih.gov/pubmed/21548960 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-2-6 |
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