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Wilson's disease: A rare autosomal recessive disorder of copper metabolism, causing copper accumulation in various organs, especially the liver and brain. ✓Genetics: 🔹Mutation in the ATP7B gene on chromosome 13. 🔹Impaired hepatic

The cholinergic system is particularly vulnerable from the early stages of the disease

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[DOI] [PMC free article] [PubMed] [Google Scholar] 316.Mitchell S., Vargas J., Hoffmann A