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This Grx-SSG intermediate is regenerated by GSH and Gor at expense of NADPH (Allen and Mieyal, 2012)

ABC transporter mutations are underrecognized causes of inherited hepatobiliary diseases that present as a spectrum of cholestatic disorders ranging from benign episodic cholestasis to progressive liver failure

10.1016/j.redox.2015.01.017 10 BelikovA

Novel-209A/G MT2A polymorphism in old patients with type 2 diabetes and atherosclerosis: relationship with inflammation (IL-6) and zinc