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Hematological and genetic profiles of persons with co-inherited heterozygous β-thalassemia and supernumerary α-globin genes.

Durga Devi SundaresanJasbir Kaur HiraSanjeev ChhabraAmita TrehanAlka Rani KhadwalPankaj MalhotraPrashant SharmaReena Das
Published in: European journal of haematology (2023)
state for the first time in such genotypically-complex Indian cases. Supernumerary α-genes should be suspected in all βTT with disproportionate clinical symptoms, mild-to-moderately elevated HbF, and unexplained anisopoikilocytosis.
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