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The disease is caused by a mutation in the ATP7B gene, which codes for a protein that facilitates the incorporation of copper into proteins (such as ceruloplasmin) and also the transportation of copper into vesicles that allow it to be secreted in bile.1 The critical effect of a mutation in ATP7B is diminished copper secretion into bile, which leads to excess copper accumulation in the hepatocyte

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The diversity of metabolites, from water-soluble compounds such as glycosides to fat-soluble constituents such as carotenoids and fats, demonstrates the chemical complexity of the plant (Zhang et al