Clinical variability and molecular characterization of Hbs/Gγ (Aγδβ)0-thal and Hbs/HPFH in Indian sickle cell disease patients: AIIMS experience
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DOI: 10.1080/16078454.2019.1579985
Abstract: ABSTRACT Introduction: In sickle cell disease (SCD) patients, among the predictors of survival, HbF levels play a significant role in lowering the morbidity and mortality. Coinheritance of δβ thalassemia and hereditary persistence of fetal hemoglobin… read more here.
Keywords: hbs; thal; hbs hpfh; disease ... See more keywords