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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,...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC407820/ https://ncbi.nlm.nih.gov/pubmed/15096575 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkh535 |
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