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From FMRP Function to Potential Therapies for Fragile X Syndrome
Fragile X syndrome (FXS) is caused by mutations in the fragile X mental retardation 1 (FMR1) gene. Most FXS cases occur due to the expansion of the CGG trinucleotide repeats in the 5′ untranslated region (UTR) of FMR1, which leads to hypermethylation and in turn silences the expression of FMRP (frag...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4024105/ https://ncbi.nlm.nih.gov/pubmed/24346713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11064-013-1229-3 |
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