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Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein
Loss of FMR1 gene function results in fragile X syndrome (FXS), the most common heritable form of intellectual disability. The protein encoded from this locus (FMRP) is an RNA binding protein thought to primarily act as a translational regulator, however recent studies implicate FMRP in other mechan...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2011
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3225737/ https://ncbi.nlm.nih.gov/pubmed/22037499 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nn.2950 |
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