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One of its most common hereditary forms, spinocerebellar ataxia type 3 (SCA3), stems from a genetic mutation in the ATXN3 gene and progressively damages the cerebellum

The unexpected changes in glutathione reductase (GR) activity in children with ASD diagnosis could be explained by the fact that GR activity is sufficient to maintain an expected GSH/GSSG ratio under physiological conditions when compared to levels in neurotypical children used as controls