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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...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2007
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2018618/ https://www.ncbi.nlm.nih.gov/pubmed/17693432 http://dx.doi.org/10.1093/nar/gkm581 |