Diversity of α‐globin mutations and clinical presentation of α‐thalassemia in Israel

α‐Thalassemia is among the world's most common single gene disorders, caused primarily by gene deletions. In Israel, where αo‐trait thalassemia is uncommon, it is of particular importance because of its phenotypic interactions with β‐thalassemia in hetero‐ and homozygotes. In a study of 232 ind...

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