The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
The fragile X mental retardation syndrome is associated with the expansion of trinucleotide 5'-d(CGG)-3' repeats within the FMR1 gene and with hypermethylation of the cytosine residues of these repeats. The expansion and hypermethylation may account for the suppression of the transcription of the FM...
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| Publicado no: | Proc Natl Acad Sci U S A |
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| Principais autores: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1994
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC43907/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8197163/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.11.4950 |
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