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Article

Genotype-Phenotype Correlation of Β-Globin Mutations and Hematological Parameters in Iraqi Β-Thalassemia Patients.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology - 31 Jul 2026

Jasim Hamsa Ahmed, Mohammed Hind Adnan, Al-Omairi Raghda

Abstract excerpt

BACKGROUND/AIMS: β-Thalassemia is a common hemoglobin disorder distributed worldwide and caused by mutations in the HBB gene that reduce or abolish β-globin chain synthesis, resulting in chronic hemolytic anemia, ineffective erythropoiesis, and variable clinical severity. Although the molecular spectrum of β-thalassemia has been extensively investigated, data correlating β-globin mutations with hematological...

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Identifiers

PMID: 42536033
DOI: 10.33594/000000879

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HBB

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Genotype-Phenotype Correlation of Β-Globin Mutations and Hematological Parameters in Iraqi Β-Thalassemia Patients.PMID 42536033Read ↗

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