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

HFE gene mutations, serum ferritin level, transferrin saturation, and their clinical correlates in a Korean population.

Digestive diseases and sciences - 1 Apr 2009

Lee Sang Hyub, Kim Jin-Wook, Shin So Hyun, Kang Kyoung Phil, Choi Hyun Cheol, Choi Sung Hee, Park Kyoung Un, Kim Hyun Young, Kang Weechang, Jeong Sook-Hyang

Abstract excerpt

The aim of this study was to investigate HFE gene mutations, blood iron indices, and their clinical correlates in a Korean population. In 484 prospectively enrolled health-check examinees, HFE gene mutations and iron indices with clinical and laboratory variables were analyzed. Although neither the C282Y nor S65C gene mutation were found, the H63D heterozygote was detected in 41 subjects (8.5%). The mean serum...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Ferritins

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

Share to Hemochromatosis Protein

Share to Histocompatibility Antigens Class I

Share to Mutation, Missense

Share to Transferrin

Source

Identifiers

PMID: 18683048
DOI: 10.1007/s10620-008-0432-6

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

HFE gene mutations, serum ferritin level, transferrin saturation, and their clinical correlates in a Korean population.PMID 18683048Read ↗

An epidemiologic study on the incidence and significance of HFE mutations in a Korean cohort with nonalcoholic fatty liver disease.Semantic proximity Read ↗

Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.Semantic proximity Read ↗

HFE gene mutation, C282Y causing hereditary hemochromatosis in Caucasian is extremely rare in Korean population.Semantic proximity Read ↗

Prevalence of HFE mutations and relation to serum iron status in patients with chronic hepatitis C and patients with nonalcoholic fatty liver disease in Taiwan.Semantic proximity Read ↗

HFE Genotype, Ferritin Levels and Transferrin Saturation in Patients with Suspected Hereditary Hemochromatosis.Semantic proximity Read ↗

HFE Gene Mutations and Iron Status in 100 Healthy Polish Children.Semantic proximity Read ↗

Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations.Semantic proximity Read ↗

Mutant HFE genotype leads to significant iron overload in patients with liver diseases from western Romania.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 ↗

Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.Semantic proximity Read ↗

HFE gene mutation, chronic liver disease, and iron overload In Turkey.Semantic proximity Read ↗

Frequencies of C282Y and H63D mutations and transferrin saturation indices in the Korean population.Semantic proximity Read ↗

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