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More research is needed to conclude if supplementing with this vitamin can improve memory in those without a deficiency

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Toxicol Appl Pharmacol 219 (2-3): 181

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3.1 Syndromes caused by mtDNA and nDNA point mutations 3.1.1 Leigh syndrome Leigh syndrome (LS) is a rare inherited neurological disorder that primarily affects infants and young children, caused by mutations in more than 75 genes of both mitochondrial and nuclear DNA (Lee et al., 2020)

It is often explored in laboratory settings focused on cellular activity and regeneration-related research