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Article

HFE mutations in patients with hereditary haemochromatosis in Sweden.

Journal of internal medicine - 1 Mar 1998

Cardoso E M, Stål P, Hagen K, Cabeda J M, Esin S, de Sousa M, Hultcrantz R

Abstract excerpt

OBJECTIVE: To determine the frequency of mutations (C282Y and H63D) in a newly identified gene HFE in patients with hereditary haemochromatosis (HH) in Sweden. DESIGN: Molecular genetic analyses of the HFE gene (polymerase chain reaction (PCR) followed by enzyme restriction) were performed in genomic DNA from unrelated patients with a clinical diagnosis of HH and in healthy subjects. SETTINGS: Patients with HH...

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Source

Identifiers

PMID: 9627157
DOI: 10.1046/j.1365-2796.1998.00270.x

Genes

HFE

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.

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HFE mutations in patients with hereditary haemochromatosis in Sweden.PMID 9627157Read ↗

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

Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls.Semantic proximity Read ↗

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