https://www.selleckchem.com/GSK-3.html
In this study, we report a Tunisian newborn boy referred for neonatal hemolytic anemia with yellowish skin and enlarged spleen due to coinheritance of hemoglobin O (HbO) Arab and β-thalassemia. Hematological parameters were collected using an automated blood cell counter. The amounts of Hb fractions were measured by capillary electrophoresis of Hb. Amplification and sequencing of the gene were performed by Sanger's method. Family study and genetic analysis revealed that the proband was a carrier of two hemoglobinopathies HbO Arab and β -thalass
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