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Mitochondrial alterations accompanied by oxidative stress conditions in skin fibroblasts of Huntington’s disease patients
Huntington disease (HD) is an autosomal dominant neurodegenerative disorder manifesting as progressive impairment of motor function and different neuropsychiatric symptoms caused by an expansion of CAG repeats in huntingtin gene (HTT). Mitochondrial dysfunction and bioenergetic defects can contribut...
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| Publicado en: | Metab Brain Dis |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Springer US
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6244791/ https://ncbi.nlm.nih.gov/pubmed/30120672 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11011-018-0308-1 |
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