Wilson's disease.

doi:10.1016/s1089-3261(05)70362-7

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Article

Wilson's disease.

Clinics in liver disease - 1 Feb 1998

Ferenci P

Abstract excerpt

Wilson's disease is an autosomal, recessive-inherited disorder of impaired biliary copper excretion that results in the accumulation of copper in various organs including the liver, the cornea and the brain. The Wilson's disease gene on chromosome 13 codes for a copper transporting P-type ATPase-ATP7B. More than 60 mutations of this gene have been described. The diagnosis of Wilson's disease is based on clinical...

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PMID: 15560044
DOI: 10.1016/s1089-3261(05)70362-7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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