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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)

This research resulted in the development of Copper Amino Isolate Serum with an exceptionally lightweight texture, and later, Copper Amino Isolate Lipid 1% which integrated a modified form of GHK-Cu that helps improve the technology's affinity with the skins lipid barrier for optimized delivery

Lassgue, B

Meadowfoam Oil nourishes and softens skin

doi: 10.1038/s41401-021-00830-1 99 FuTWangSLiuJCaiELiHLiPet al