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An Origin of DNA Replication in the Promoter Region of the Human Fragile X Mental Retardation (FMR1) Gene
Fragile X syndrome, the most common form of inherited mental retardation in males, arises when the normally stable 5 to 50 CGG repeats in the 5′ untranslated region of the fragile X mental retardation protein 1 (FMR1) gene expand to over 200, leading to DNA methylation and silencing of the FMR1 prom...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Microbiology
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1800797/ https://ncbi.nlm.nih.gov/pubmed/17101793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.01382-06 |
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