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Article

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

Human molecular genetics - 15 Jun 2003

Halsall David J, McFarlane Ian, Luan Jian'an, Cox Timothy M, Wareham Nicholas J

Abstract excerpt

Diabetes mellitus is a recognized consequence of hereditary haemochromatosis. Whether the common HFE mutations, that associate with this condition and pre-dispose to increases in serum iron indices, are over-represented in diabetic populations remains controversial. We present data from the largest case-control study of the C282Y and H63D HFE allele frequencies in typical type 2 diabetes mellitus, as defined by...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12783844
DOI: 10.1093/hmg/ddg149

Genes

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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