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COPPER DYSREGULATION RELATED TO ATP7B GENETIC ISSUES IN WILSON DISEASE Excessive hepatic copper deposition in Wilson disease results from impaired biliary excretion of excess copper due to dysfunction of the ATP7B gene [20,21,24,27]

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doi: 10.1089/lrb.2018.0013 163 UbellackerJMTasdoganARameshVShenBMitchellECMartin-SandovalMSet al