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Article

Rare hemoglobin variants in Tunisian population.

International journal of laboratory hematology - 1 Apr 2015

Zorai A, Moumni I, Mosbahi I, Douzi K, Chaouachi D, Guemira F, Abbes S

Abstract excerpt

During the last 30 years, many studies concerning hemoglobinopathies were realized among Tunisians. More than twenty different thalassemic alleles were detected on the β-globin gene, and less are affecting the α-globin genes. Unusual hemoglobin (Hb) variants other than Hb S, Hb C, and Hb O-arab, which are the most frequent variants in Tunisia, were also detected. Eight Tunisian subjects were studied at phenotypic...

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Identifiers

PMID: 24905386
DOI: 10.1111/ijlh.12259

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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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