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The molecular mechanisms that underlie fragile X-associated premature ovarian insufficiency: is it RNA or protein based?
The FMR1 gene contains a polymorphic CGG trinucleotide sequence within its 5′ untranslated region. More than 200 CGG repeats (termed a full mutation) underlie the severe neurodevelopmental condition fragile X syndrome, while repeat lengths that range between 55 and 200 (termed a premutation) result...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566375/ https://www.ncbi.nlm.nih.gov/pubmed/32777047 http://dx.doi.org/10.1093/molehr/gaaa057 |