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Article

Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients.

Hemoglobin - 1 Mar 2020

Azarkeivan Azita, Cohan Nader, Niazkar Hamid Reza, Azizi Arsalan, Rad Fariba

Abstract excerpt

Hb S (HBB: c.20A>T) and α- and/or β-thalassemia (α- and/or β-thal) coinheritance is a common genetic disorder in regions with a high prevalence of thalassemia and sickle cell disease. The clinical manifestations of this coinheritance vary from mild to severe complications. Iran is a country with a high incidence of thalassemia and sickle cell disease. This study aimed to evaluate the coinheritance of sickle cell...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 32370567
DOI: 10.1080/03630269.2020.1757462

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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