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5.3 Huntingtons disease Huntingtons disease is a rare autosomal dominant hereditary neurodegenerative disease

Boosting levels of this antioxidant can reduce the progression of the illness and the symptoms

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Our analysis showed no significant differences in the expression of mitochondrial genes or related pathways between wild-type and hepsin / mice at any time point, as determined by transcriptome analysis, pathway enrichment, and GSEA

These findings highlight its broad pharmacological potential and establish a scientific basis for future combined Chinese and Western therapeutic strategies