Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1: C.119_121delCCA Mutation and HBA2: C.*94A  >  G Mutation

.

Source: Hemoglobin - April 17, 2024 Category: Hematology Authors: Nada AssafRoba El ZibaouiCarla MonsefTania Abi NassifMiguel AbboudSoha Yazbeka Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanonb Faculty of Medicine, American University of Beirut, Beirut, Leba Source Type: research