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Wilson's disease: A rare autosomal recessive disorder of copper metabolism, causing copper accumulation in various organs, especially the liver and brain. ✓Genetics: 🔹Mutation in the ATP7B gene on chromosome 13. 🔹Impaired hepatic
Abstract Oxidative stress and TNFα are critically involved in the initiation and progression of non-alcoholic fatty liver disease (NAFLD)
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The yield for Cr FAP65AH1 was lower than that obtained for Cr FAP65AH1V12P, and the reason for this is not known (Fig
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