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Article

S65C and other mutations in the haemochromatosis gene in the Czech population.

Folia biologica - 1 Jan 2005

Cimburová M, Půtová I, Provazníková H, Pintérová D, Horák J

Abstract excerpt

HFE-linked hereditary haemochromatosis is a common autosomal recessive disease among Caucasians. The primary pathogenetic mechanism is excessive absorption of iron, which is deposited in various organs with their subsequent damage. In 1996 the gene responsible for haemochromatosis was detected--t...

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Identifiers

PMID: 16419611

Genes

HFE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16419611-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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S65C and other mutations in the haemochromatosis gene in the Czech population.PMID 16419611Read ↗

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