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Wilson disease is a genetic disorder resulting in excessive accumulation of copper in the body. People with Wilson disease are unable to excrete copper, therefore, over a period of time copper slowly The Effect of the Human Peptide GHK on Gene Expression Relevant to Nervous System Function and Cognitive Decline PMC ghk cu wilson's disease contraindication Comprehensive Pharmacological Management of Wilson's Disease: Mechanisms, Clinical Strategies, and Emerging Wilson disease: At the crossroads between genetics and epigeneticsA review of the evidence ScienceDirect Wilson's Disease Treating a Rare But Curable Movement Disorder Dr Mitesh Chandarana Wilson's disease: diagnosis and management The Pharmaceutical Journal
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