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Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 2a genetic neurodegenerative disorder due to a CAG repeat expansion mutation in the ATXN2 gene coding for the protein ataxin-2 63 has been associated to oxidative stress, in particular due to alterations in the enzymatic activity of antioxidant enzymes including GSTs 64
Dietary improvements support long-term health and may lead to gradual increases over several weeks
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Liposomes are microscopic spheres made of the same natural phospholipids that make up our cell membranes with an active ingredient like glutathione contained and protected in the sphere's center
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