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Article

Cardiac hemochromatosis in an HFE His63Asp (187C->G) heterozygote.

The Canadian journal of cardiology - 1 Aug 2004

Winer Daniel, Silversides Candice, Israel Noobar, Rinne Claus, Chang Wilson S C, Butany Jagdish

Abstract excerpt

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Topics

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Share to Biopsy, Needle
Share to Echocardiography, Doppler
Share to Genes, MHC Class I
Share to Hemochromatosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Histocompatibility Antigens Class I

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Source

Identifiers

PMID: 15332145

Genes

HFE

Provenance

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

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cardiac hemochromatosis in an HFE His63Asp (187C->G) heterozygote.PMID 15332145Read ↗

Clinical haemochromatosis in HFE mutation carriers.Semantic proximity Read ↗

Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.Semantic proximity Read ↗

Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.Semantic proximity Read ↗

The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis.Semantic proximity Read ↗

Haemochromatosis: diagnosis and management after the cloning of the HFE gene.Semantic proximity Read ↗

Is H63D a 'minor' HFE polymorphism?Semantic proximity Read ↗

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.Semantic proximity Read ↗

Molecular characterisation and diagnosis of Hb J-Taichung (129[H7]Ala-->Asp) in a Taiwanese family subject.Semantic proximity Read ↗

Diagnosis and management of haemochromatosis since the discovery of the HFE gene: a European experience.Semantic proximity Read ↗

Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations.Semantic proximity Read ↗

Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.Semantic proximity Read ↗

New HJV mutation in a patient with hyperferritinemia and H63D homozygosity for the HFE gene.Semantic proximity Read ↗

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