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The molecular basis of copper transport diseases: Trends in Molecular Medicine Wilson Disease Hereditary Ocular Diseases What is Wilson's Disease? Wilson's disease is a rare genetic disorder that prevents the body from properly eliminating excess copper. This condition leads to copper accumulation in vital organs, primarily the liver ghk cu copper overload risk wilson's disease What is Disease? Wilson's is a rare genetic disorder Wilson disease and related copper disorders ScienceDirect Wilson's Disease: A Comprehensive Review of the Molecular Mechanisms
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