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Article

Toxic milk mice models of Wilson's disease.

Molecular biology reports - 1 Feb 2021

Hadrian Krzysztof, Przybyłkowski Adam

Abstract excerpt

Wilson's disease (WD) is a rare genetic disorder inherited as an autosomal recessive trait. The signs and symptoms of this disease are related to dysfunctional ATP7B protein which leads to copper accumulation and cellular damage. The organs that are most commonly affected by WD are the liver and brain. The dysfunctional ATP7B homolog has previously been identified in many different species, including two...

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Identifiers

PMID: 33590415
DOI: 10.1007/s11033-021-06192-5
PMCID: PMC7925478

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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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