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In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation
Fragile X syndrome (FXS), caused by loss of the Fragile X Mental Retardation 1 (FMR1) gene product (FMRP), is the most common heritable cause of intellectual disability and autism spectrum disorders. It has been long hypothesized that the phosphorylation of serine 500 (S500) in human FMRP controls i...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3263990/ https://ncbi.nlm.nih.gov/pubmed/22080836 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr527 |
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