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AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats
BACKGROUND: Fragile X Syndrome (FXS), the most common inherited form of mental retardation, is caused by expansion of a CGG/CCG repeat tract in the 5′-untranslated region of the fragile X mental retardation (FMR1) gene, which changes the functional organization of the gene from euchromatin to hetero...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2013
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3870987/ https://ncbi.nlm.nih.gov/pubmed/24261641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2091-14-33 |
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