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Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease
Expanded CGG-repeats have been linked to neurodevelopmental and neurodegenerative disorders, including the fragile X syndrome and fragile X-associated tremor/ataxia syndrome (FXTAS). We hypothesized that as of yet uncharacterised CGG-repeat expansions within the genome contribute to human disease. T...
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| Publicat a: | Sci Rep |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7844047/ https://ncbi.nlm.nih.gov/pubmed/33510257 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-82050-5 |
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