Thalassemias result from genetic defects that impair the synthesis of either the alpha or beta globin chains of hemoglobin.
What happens in human Thalassemias? reduce $\alpha$ - globin synthesis reduce $\beta$ - globin synthesis enhance $\alpha$ and $\beta$ - globin synthesis
Asked in TNPSC CS Prelims 2019 · Topic: Genetic Disorders (Mendelian Disorders: Autosomal Dominant, Autosomal Recessive, X-linked)
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