Nalaganje...
DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome
Among the inherited causes of intellectual disability and autism, Fragile X syndrome (FXS) is the most frequent form, for which there is currently no cure. In most FXS patients, the FMR1 gene is epigenetically inactivated following the expansion over 200 triplets of a CGG repeat (FM: full mutation)....
Shranjeno v:
| izdano v: | Biomolecules |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI
2021
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7920310/ https://ncbi.nlm.nih.gov/pubmed/33669384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biom11020296 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|