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Article

Haemochromatosis-causing mutations C282Y and H63D are not risk factors for coronary artery disease in Caucasians with type 2 diabetes.

Folia biologica - 1 Jan 2004

Zorc M, Hruskovicová H, Petrovic M Globocnik, Milcić M, Peterlin B, Petrovic D

Abstract excerpt

Iron metabolism might be involved in the pathogenesis of CAD, and C282Y and H63D mutations in the HFE gene are associated with increased serum iron levels and net iron accumulation. The aim of this study was to look for a relationship between the C282Y and H63D gene mutations of the HFE gene and coronary artery disease (CAD) in a group of patients with type 2 diabetes lasting more than 10 years. The C282Y and...

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Source

Identifiers

PMID: 15222129

Genes

CAD
HFE

Provenance

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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Haemochromatosis-causing mutations C282Y and H63D are not risk factors for coronary artery disease in Caucasians with type 2 diabetes.PMID 15222129Read ↗

Haemochromatosis gene mutations and risk of coronary artery disease.Semantic proximity Read ↗

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Prevalence, characteristics, and prognostic significance of HFE gene mutations in type 2 diabetes: the Fremantle Diabetes Study.Semantic proximity Read ↗

A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes.Semantic proximity Read ↗

Prevalence of coronary heart disease associated with HFE mutations in adults attending a health appraisal center.Semantic proximity Read ↗

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Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study.Semantic proximity Read ↗

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