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

[The prevalence of the Cys282Tyr mutation in the hemochromatosis gene in Cantabria in patients diagnosed with hereditary hemochromatosis].

Medicina clinica - 10 Apr 1999

Fábrega E, Castro B, Sánchez-Castro L, Benito A, Fernández-Luna J L, Pons-Romero F

Abstract excerpt

BACKGROUND: The aim of our study was to evaluate the prevalence of Cys282Tyr mutation in patients with genetic haemochromatosis (GH) in Cantabria. PATIENTS AND METHODS: The HFE Cys282Tyr mutation was determined in a cohort of 60 patients with GH and 213 controls. RESULTS: The frequency of the Cys282Tyr mutation in control individuals was 4.4%. Sixty-seven percent of patients with GH were homozygous for the...

Read the complete abstract on PubMed

Topics

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

Share to Cysteine
Share to DNA Primers

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Hemochromatosis

Share to Polymerase Chain Reaction

Share to Prevalence

Share to Tyrosine

Source

Identifiers

PMID: 10320958

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 · 11 closest

[The prevalence of the Cys282Tyr mutation in the hemochromatosis gene in Cantabria in patients diagnosed with hereditary hemochromatosis].PMID 10320958Read ↗

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

Hemochromatosis gene HFE Cys282Tyr mutation analysis in a cohort of Northeast German hospitalized patients supports assumption of a North to South allele frequency gradient throughout Germany.Semantic proximity Read ↗

[The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].Semantic proximity Read ↗

Haemochromatosis gene mutations Cys282Tyr and His63Asp are not increased in Type 2 diabetic patients compared with the Canterbury (New Zealand) general population.Semantic proximity Read ↗

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis.Semantic proximity Read ↗

Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca.Semantic proximity Read ↗

High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population ‐implications for haemochromatosisSemantic proximity Read ↗

Ethnic differences in the HFE codon 282 (Cys/Tyr) polymorphism.Semantic proximity Read ↗

Frequency of the C282Y mutation of hemochromatosis in five French populations.Semantic proximity Read ↗

[Analysis of the hemochromatosis gene (HFE) mutations, C282Y and H63D, in the populations of Central Asia].Semantic proximity Read ↗

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda.Semantic proximity Read ↗

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