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Background and objectivesBombay phenotype is characterized by the lack of H substance both on red blood cell (RBC) surface and in body secretions. Mutations of fucosyltransferase 1 (FUT1) and fucosyltransferase 2 (FUT2) genes are resulted in this rare phenotype.
Materials and methodsFive unrelated patients were tested by hemagglutination and adsorption/elution techniques for the presence of ABH antigens...
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