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Molecular Biomarkers in Fragile X Syndrome
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability (ID) and a known monogenic cause of autism spectrum disorder (ASD). It is a trinucleotide repeat disorder, in which more than 200 CGG repeats in the 5’ untranslated region (UTR) of the fragile X mental retardation...
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| Publicado no: | Brain Sci |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6562871/ https://ncbi.nlm.nih.gov/pubmed/31035599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/brainsci9050096 |
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