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Postsynaptic FMRP Regulates Synaptogenesis In Vivo in the Developing Cochlear Nucleus
A global loss of the fragile X mental retardation protein (FMRP; encoded by the Fmr1 gene) leads to sensory dysfunction and intellectual disabilities. One underlying mechanism of these phenotypes is structural and functional deficits in synapses. Here, we determined the autonomous function of postsy...
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| 出版年: | J Neurosci |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Society for Neuroscience
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6052239/ https://ncbi.nlm.nih.gov/pubmed/29950504 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0665-18.2018 |
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