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Interactions of the G quartet forming semaphorin 3F RNA with the RGG box domain of the fragile X protein family
Fragile X syndrome, the most common cause of inherited mental retardation, is caused by the transcriptional silencing of the fmr1 gene due to an unstable expansion of a CGG trinucleotide repeat and its subsequent hypermethylation in its 5′ UTR. This gene encodes for the fragile X mental retardation...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2007
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2018618/ https://ncbi.nlm.nih.gov/pubmed/17693432 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkm581 |
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