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Wilsons disease (WD) is a rare autosomal recessive genetic disorder characterised by the accumulation of copper in various body tissues, particularly the brain, liver and corneas of the eyes[1]

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(2022) reported that enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase was strongly correlated with individual trace organic chemical transformation in the water biofiltration process

It is used as a performance-enhancing drug and is banned by the World Anti-doping Agency