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Due to the dualistic role of ATP7B in both the synthesis of the copper-containing protein ceruloplasmin and biliary excretion of copper, defects in its function lead to copper accumulation in the liver and other organs that express ATP7B [16,32,40] because both functions of ATP7B are impaired in Wilson disease due to ATP7B gene mutation [25,26,31,33,41]
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[PMC free article: PMC1642707] [PubMed: 16815800] 113
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