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The fragile X mental retardation protein has nucleic acid chaperone properties
The fragile X syndrome is the most common cause of inherited mental retardation resulting from the absence of the fragile X mental retardation protein (FMRP). FMRP contains two K-homology (KH) domains and one RGG box that are landmarks characteristic of RNA-binding proteins. In agreement with this,...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Nucleic Acids Res |
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| Prif Awduron: | , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Oxford University Press
2004
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC407820/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15096575/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/gkh535 |
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