ghk-cu wilson's disease β Wilson β Autosomal recessive disorder of copper metabolism, leading to toxic accumulation in liver, brain, and eyes. πΉ Genetics βοΈ Mutation in ATP7B gene (chromosome 13) βοΈ β Copper excretion Wilson disease (Hepatolenticular Degeneration)- Copper
Wilson disease (Hepatolenticular Degeneration) Copper Causes, Symptoms, Diagnosis, Treatment The history of Wilson disease PMC Understanding Wilson's Disease Genetic Disorders: Wilson's Disease MedRelatable
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