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Intravenous vitamin C in the treatment of allergies: an interim subgroup analysis of a long-term observational study - PMC

ACP is a rare autosomal recessive disorder caused by mutations in the ceruloplasmin gene that lead to reduced ferroxidase activity

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The identification of tubulins and protein disulfide-isomerase A3 across both cell lines suggests that X(PC) may promote cell death by targeting structural and apoptotic regulatory proteins, thereby mimicking broad caspase proteolysis activity during programmed cell death

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