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Non-coding RNA in Fragile X Syndrome and Converging Mechanisms Shared by Related Disorders
Fragile X syndrome (FXS) is one of the most common forms of hereditary intellectual disability. It is also a well-known monogenic cause of autism spectrum disorders (ASD). Repetitive trinucleotide expansion of CGG repeats in the 5′-UTR of FMR1 is the pathological mutation. Full mutation CGG repeats...
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| Publicado no: | Front Genet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6405884/ https://ncbi.nlm.nih.gov/pubmed/30881383 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00139 |
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