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The production of Hb F after birth is an important factor in modifying the clinical severity of beta thalassemia because an increased gamma-globin level will bind the additional a-globin and form Hb F. The objective of this project is to evaluate the association of Hb F level with phenotypic diversity of patients with beta thalassemia.
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1,200 participants in 1 patient group
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Xiangmin Xu, Prof. Dr.
Data sourced from clinicaltrials.gov
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