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HFE and Non-HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience.

Genetic testing and molecular biomarkers - 1 Jul 2024

Zarifian Yeganeh Razieh, Akbari Kelishomi Masoumeh, Ahmadpour Jenaghard Atiyeh, Salmani Banafsheh, Vahidi Zohreh, Makvand Mina, Azad Maryam, Kooshki Mahdieh, Bouraqi Yassin, Azarkeivan Azita, Najmabadi Hossein, Neishabury Maryam

Abstract excerpt

Introduction: The genetics of hereditary hemochromatosis (HH) is understudied in Iran. Here, we report the result of genetic screening of 854 individuals, referred as "suspected cases of HH," to a diagnostic laboratory in Iran over a 12-year period. Materials and Methods: From 2011 to 2012, 121 cases were screened for HH using Sanger sequencing of HFE exons. After 2012, this method was replaced by a commercial...

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PMID: 38980801
DOI: 10.1089/gtmb.2023.0764

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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