Sickle cell anemia is due to gene modificatio related to amino acid of beta second chain
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Sickle cell disease (SCD) is an autosomal recessive disorder in which a substitution of valine for glutamic acid in the β-chain hemoglobin molecule143 causes red blood cells to form sickle shapes and polymerize particularly when patients are exposed to hypoxemia or extremes of temperature or are dealing with infections.
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