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Article

The toxic milk mutation, tx, which results in a condition resembling Wilson disease in humans, is linked to mouse chromosome 8.

Genomics - 20 Sept 1995

Rauch H, Wells A J

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 8666408
DOI: 10.1006/geno.1995.9968

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The toxic milk mutation, tx, which results in a condition resembling Wilson disease in humans, is linked to mouse chromosome 8.PMID 8666408Read ↗

The toxic milk mouse is a murine model of Wilson disease.Semantic proximity Read ↗

Toxic milk mice models of Wilson's disease.Semantic proximity Read ↗

Functional studies on the Wilson copper P-type ATPase and toxic milk mouse mutant.Semantic proximity Read ↗

Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase.Semantic proximity Read ↗

A Gene Therapy Approach to Improve Copper Metabolism and Prevent Liver Damage in a Mouse Model of Wilson DiseaseSemantic proximity Read ↗

A novel gene involved in zinc transport is deficient in the lethal milk mouse.Semantic proximity Read ↗

Molecular mapping of the tubby (tub) mutation on mouse chromosome 7.Semantic proximity Read ↗

Toxic milk, a new mutation affecting cooper metabolism in the mouse.Semantic proximity Read ↗

Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transportersSemantic proximity Read ↗

High-resolution mapping of the truncate (tc) locus on mouse chromosome 6.Semantic proximity Read ↗

Localization of the twitcher (twi) mutation on mouse chromosome 12.Semantic proximity Read ↗

[Mice with mottled mutation--a model for defective copper metabolism in humans].Semantic proximity Read ↗

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