Molecular and hematological spectrum of α-thalassemia in Saudi patients

α-thalassemia (α-thal) is a genetic disorder characterized by a decreased synthesis of α-globin chains. A deletion mutation most often causes it in one or more α-globin chains. No comprehensive characterization studies have been conducted on α-thal patients in the Saudi population. Therefore, this...

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Bibliographic Details
Main Authors: Raed Alserihi, Sarah Alswat, Heba Alkhatabi, Haitham M.H. Qutob, Elrashed B. Yasin, Talal Qadah
Format: Article
Language:English
Published: PAGEPress Publications 2024-11-01
Series:Italian Journal of Medicine
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Online Access:https://www.italjmed.org/ijm/article/view/1837
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