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Article

Frequency of beta-thalassemia or beta-hemoglobinopathy carriers simultaneously affected with alpha-thalassemia in Iran.

Clinical laboratory - 1 Jan 2014

Alizadeh Shaban, Bavarsad Mahsa Shanaki, Dorgalaleh Akbar, Khatib Zahra Kashani, Dargahi Hossein, Nassiri Nhaid, Hamid Fatemeh, Rahim Fakher, Jaseb Kaveh, Saki Najmaldin

Abstract excerpt

BACKGROUND: Beta-thalassemias are prevalent heritable single gene disorders affecting the quantity of the hemoglobin molecule. Rarely, a co-inheritance of these impairments with alpha-thalassemia and/or a hemoglobinopathy occurs and makes an important double heterozygote or homozygous state. Thus finding these cases is essential for genetic counseling. The present study aimed to identify the prevalence of...

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PMID: 25016698
DOI: 10.7754/clin.lab.2013.130306

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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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