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The most compelling studies of efficacy have been done in cell cultures and small animals
At the most basic level, glutathione cycles between a reduced form (GSH) and an oxidized form (GSSG)
Primary carnitine deficiency PCD is a rare genetic disease caused by mutations in the SLC22A5 gene, which leads to dysfunction of the carnitine transporter OCTN2, thereby hindering the entry of carnitine from the blood into cells and the reabsorption of carnitine by the kidneys
Free radicals in the physiological control of cell function
14% in placebo-treated individuals
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