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The Pathophysiology of Fragile X (and What It Teaches Us about Synapses)
Fragile X is the most common known inherited cause of intellectual disability and autism, and it typically results from transcriptional silencing of FMR1 and loss of the encoded protein, FMRP (fragile X mental retardation protein). FMRP is an mRNA-binding protein that functions at many synapses to i...
Shranjeno v:
| izdano v: | Annu Rev Neurosci |
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| Main Authors: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2012
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4327822/ https://ncbi.nlm.nih.gov/pubmed/22483044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1146/annurev-neuro-060909-153138 |
| Oznake: |
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