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Article

A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran.

Hemoglobin - 1 Jan 2017

Eftekhari Hajar, Tamaddoni Ahmad, Mahmoudi Nesheli Hassan, Vakili Mohsen, Sedaghat Sadegh, Banihashemi Ali, Azizi Mandana, Youssefi Kamangar Reza, Akhavan-Niaki Haleh

Abstract excerpt

α-Thalassemia (α-thal) is the most common monogenic disease that is caused by the absence or reduced expression of α-globin genes. The aim of this study was to investigate common α-globin mutations and their associated haplotypes in four northern provinces of Iran (Gilan, Mazandaran, Golestan, Khorasan). One thousand, one hundred and ninety-one persons were tested for α-thal mutations by gap-polymerase chain...

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Identifiers

PMID: 28385057
DOI: 10.1080/03630269.2017.1299753

Genes

HBA2

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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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