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Article

Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest Iran.

Hemoglobin - 1 Jan 2010

Galehdari Hamid, Salehi Bahaoddin, Azmoun Somaiyeh, Keikhaei Bijan, Zandian Khoda Morad, Pedram Mohammad

Abstract excerpt

β-Thalassemia (β-thal) is characterized by reduction or absence of β-globin gene expression. We describe the spectrum of mutations observed in a large cohort of β-thal carriers in Khuzestan, Southwest Iran. All together 1,241 blood samples from individuals with decreased mean corpuscular volume (MCV) and elevated Hb A(2) levels, were analyzed either by reverse dot-blot or by direct sequencing of the HBB gene. We...

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Identifiers

PMID: 20854120
DOI: 10.3109/03630269.2010.514153

Genes

HBB

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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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