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There are an estimated 300 million people in the world recognized as carriers of hemoglobin S (Hb S), a condition resulting from the substitution of glutamic acid for valine at position 6 of the β-globin gene on the short arm of chromosome 11, which are characterized by the inheritance of a normal hemoglobin A gene from one parent and an abnormal mutated gene from the other parent (AS), unlike homozygous individuals in which both mutated genes are present (SS). .
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