Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Distribution of the C282Y and H63D polymorphisms in hereditary hemochromatosis patients from the French Basque Country.

Annals of hematology - 1 Feb 2005

Bauduer F, Scribans C, Degioanni A, Renoux M, Dutour O

Abstract excerpt

The distribution of HFE mutations was studied in patients from the French Basque Country with hereditary hemochromatosis (HH). The C282Y mutation was underrepresented but H63D seemed to demonstrate the highest prevalence when compared with other European countries. In addition, symptomatic HH was rarer in autochthonous Basques. This profile is interesting to consider in view of population genetics and should be...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Europe
Share to France
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemochromatosis

Share to Molecular Epidemiology

Share to Mutation, Missense

Share to Polymorphism, Genetic

Share to Prevalence

Source

Identifiers

PMID: 15503019
DOI: 10.1007/s00277-004-0957-5

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Distribution of the C282Y and H63D polymorphisms in hereditary hemochromatosis patients from the French Basque Country.PMID 15503019Read ↗

HFE gene mutations analysis in Basque hereditary haemochromatosis patients and controls.Semantic proximity Read ↗

Genetic hemochromatosis is a rare disease entity among French Basques: a center-based study from the general hospital of Basque County.Semantic proximity Read ↗

Significance of H63D homozygosity in a Basque population with hemochromatosis.Semantic proximity Read ↗

Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina.Semantic proximity Read ↗

Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in a cohort of 1,000 neonates in Madrid (Spain).Semantic proximity Read ↗

C282Y and H63D mutation frequencies in a population from central Spain.Semantic proximity Read ↗

Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis.Semantic proximity Read ↗

Distribution of HFE C282Y and H63D mutations in the Balearic Islands (NE Spain).Semantic proximity Read ↗

Uncommon mutations and polymorphisms in the hemochromatosis gene.Semantic proximity Read ↗

Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.Semantic proximity Read ↗

Frequency of HFE mutations among Turkish blood donors according to transferrin saturation: genotype screening for hereditary hemochromatosis among voluntary blood donors in Turkey.Semantic proximity Read ↗

Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.