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Repeat-mediated epigenetic dysregulation of the FMR1 gene in the fragile X-related disorders
The fragile X-related disorders are members of the Repeat Expansion Diseases, a group of genetic conditions resulting from an expansion in the size of a tandem repeat tract at a specific genetic locus. The repeat responsible for disease pathology in the fragile X-related disorders is CGG/CCG and the...
Tallennettuna:
| Julkaisussa: | Front Genet |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4452891/ https://ncbi.nlm.nih.gov/pubmed/26089834 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2015.00192 |
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