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Leigh syndrome, a rare and severe pediatric mitochondrial disease, is most commonly caused by mutations in complex I or IV of OXPHOS, although defects in complexes II and V have also been reported [11, 12]
Its a naturally occurring compound your body already uses to convert fat into energy
The lowest level of antioxidant intake or tissue concentration results in nutrient deficiency if the antioxidant is essential (vitamins and minerals)
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Obesity and age-related alterations in the gene expression of zinc-transporter proteins in the human brain
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