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G6PD deficiency is a common inherited disorder characterized by hemolysis and has been suggested to be associated with the onset of ALF in case reports[33]
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Key finding: Upregulated SOD, glutathione S-transferase, and endogenous antioxidant genes while suppressing pro-oxidant expression reversing age-related oxidative decline
[11] [6] Rare but serious reactions: Although uncommon, anaphylaxis (severe allergic reaction) can occur
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