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The combination of variants linked to a slightly increased risk of liver damage could add together to increase the risk more significantly
1c,d) and was previously suggested as a candidate for a potential activator site, first, because its positive charge might stabilize or bind GSH as GS , and, second, because of its evolutionary conserved position that is equivalent to the GSH-interacting catalytic residue of glutathione transferases 3
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Presented for research literature review only Mor M et al
Research peptides are not FDA-approved for human use unless specifically noted
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