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Altered Redox Mitochondrial Biology in the Neurodegenerative Disorder Fragile X-Tremor/Ataxia Syndrome: Use of Antioxidants in Precision Medicine
A 55–200 expansion of the CGG nucleotide repeat in the 5’-UTR of the fragile X mental retardation 1 gene (FMR1) is the hallmark of the triplet nucleotide disease known as the “premutation” as opposed to those with >200 repeats, known as the full mutation or fragile X syndrome. Originally, premuta...
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| Publicado no: | Mol Med |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Feinstein Institute for Medical Research
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5082295/ https://ncbi.nlm.nih.gov/pubmed/27385396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2119/molmed.2016.00122 |
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