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The RNA-binding fragile-X mental retardation protein and its role beyond the brain
It is well-established that variations of a CGG repeat expansion in the gene FMR1, which encodes the fragile-X mental retardation protein (FMRP), cause the neurocognitive disorder, fragile-X syndrome (FXS). However, multiple observations suggest a general and complex regulatory role of FMRP in proce...
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| Vydáno v: | Biophys Rev |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Berlin Heidelberg
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7429658/ https://ncbi.nlm.nih.gov/pubmed/32654068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12551-020-00730-4 |
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