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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

It has not completed the clinical-trial process that approval requires

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This is due to the fact that a deficiency of this molecule manifests in increased susceptibility to oxidative stress, and the resulting damage is thought to be a key step in the onset and progression of eye diseases [48]