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Neurotherapeutics 7(1):100114

The reference lists of the retrieved publications were also searched for additional relevant published and unpublished studies, including conference abstracts

It is considered rare, with a prevalence of approximately 1 in 30,000 individuals. Geeky Medics bundles and get discounted access to all our resources in one place Aetiology Wilsons disease is an autosomal recessive disorder caused by mutations in the ATP7B gene located on chromosome 13

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