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Functional and structural deficits at accumbens synapses in a mouse model of Fragile X
Fragile X is the most common cause of inherited intellectual disability and a leading cause of autism. The disease is caused by mutation of a single X-linked gene called fmr1 that codes for the Fragile X mental retardation protein (FMRP), a 71 kDa protein, which acts mainly as a translation inhibito...
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| 出版年: | Front Cell Neurosci |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4374460/ https://ncbi.nlm.nih.gov/pubmed/25859182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2015.00100 |
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