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Exenatide induces frataxin expression and improves mitochondrial function in Friedreich ataxia
Friedreich ataxia is an autosomal recessive neurodegenerative disease associated with a high diabetes prevalence. No treatment is available to prevent or delay disease progression. Friedreich ataxia is caused by intronic GAA trinucleotide repeat expansions in the frataxin-encoding FXN gene that redu...
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| Veröffentlicht in: | JCI Insight |
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Society for Clinical Investigation
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7098728/ https://ncbi.nlm.nih.gov/pubmed/31877117 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.134221 |
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