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Article

Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait.

European journal of haematology - 1 Apr 2005

Garewal Gurjeewan, Das Reena, Ahluwalia Jasmina, Marwaha R K

Abstract excerpt

OBJECTIVES: To determine the allele frequency in the north Indian population of the two mutations in the HFE gene, the C282Y and H63D, which are responsible for causing hereditary haemochromatosis particularly in Caucasians of north European descent. We also wanted to correlate these mutations with the iron status in beta thalassemia traits. PATIENTS AND METHODS: Sixty normal subjects and 215 individuals with...

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

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Source

Identifiers

PMID: 15777346
DOI: 10.1111/j.1600-0609.2004.00390.x

Genes

HFE

Variants

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.

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Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait.PMID 15777346Read ↗

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