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Article

Frequency of the hemochromatosis C282Y and H63D mutations in a Polish population of Slavic origin.

Medical science monitor : international medical journal of experimental and clinical research - 1 Jan 2000

Moczulski D K, Grzeszczak W, Gawlik B

Abstract excerpt

BACKGROUND: Hereditary hemochromatosis is one of the most common monogenic diseases among Caucasians. The most frequent mutation causing hemochromatosis is C282Y in the HFE gene, the highest frequency of which has been observed in populations of Celtic origin. There are no studies providing information about the frequency of the C282Y and H63D mutations in the HFE gene in populations of Slavic origin. MATERIAL...

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Source

Identifiers

PMID: 11386022

Genes

HFE

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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Frequency of the hemochromatosis C282Y and H63D mutations in a Polish population of Slavic origin.PMID 11386022Read ↗

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Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.Semantic proximity Read ↗

HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.Semantic proximity Read ↗

Celtic origin of the C282Y mutation of hemochromatosis.Semantic proximity Read ↗

Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients.Semantic proximity Read ↗

A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?Semantic proximity Read ↗

Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis.Semantic proximity Read ↗

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