Association of the Degree of Erythroid Expansion and Maturation Arrest with the Clinical Severity of β<sup>0</sup>-Thalassemia/Hemoglobin e Patients

Introduction: β-Thalassemia/hemoglobin E represents one-half of all the clinically severe β-thalassemias worldwide. Despite similar genetic backgrounds, patients show clinical heterogeneity ranging from nearly asymptomatic to transfusion-dependent thalassemia. The underlying disease modifying factor...

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Bibliographic Details
Main Authors: Thunwarat Suriyun, Woratree Kaewsakulthong, Pinyaphat Khamphikham, Sukanya Chumchuen, Suradej Hongeng, Suthat Fucharoen, Orapan Sripichai
Other Authors: Siriraj Hospital
Format: Article
Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/77729
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Institution: Mahidol University