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Article

Clinical haemochromatosis in HFE mutation carriers.

Lancet (London, England) - 3 Aug 2002

Cox Timothy, Rochette Jacques, Camaschella Clara, Walker Ann, Robson Kathryn

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Topics

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Share to Health Status
Share to Hemochromatosis
Share to Hemochromatosis Protein
Share to Histocompatibility Antigens Class I

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12241804
DOI: 10.1016/S0140-6736(02)09582-X

Genes

HFE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Clinical haemochromatosis in HFE mutation carriers.PMID 12241804Read ↗

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Pathophysiological consequences and benefits of HFE mutations: 20 years of research.Semantic proximity Read ↗

Hereditary hemochromatosis since discovery of the HFE gene.Semantic proximity Read ↗

Cardiac hemochromatosis in an HFE His63Asp (187C->G) heterozygote.Semantic proximity Read ↗

EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)Semantic proximity Read ↗

HFE gene and hemochromatosis.Semantic proximity Read ↗

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