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Article

Regulation of iron absorption in Hfe mutant mice.

Blood - 15 Aug 2002

Ajioka Richard S, Levy Joanne E, Andrews Nancy C, Kushner James P

Abstract excerpt

Hereditary hemochromatosis is most commonly caused by homozygosity for a point mutation (C282Y) in the human hemochromatosis gene (HFE). The mechanism by which HFE regulates iron absorption is not known, but the C282Y mutation results in loss of cell surface expression of the human hemachromatosi...

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Source

Identifiers

PMID: 12149232
DOI: 10.1182/blood-2001-11-0037

Genes

HFE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12149232-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Regulation of iron absorption in Hfe mutant mice.PMID 12149232Read ↗

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