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Background
The Am phenotype, which arises from mutations of the α‐1,3‐N‐acetylgalactosaminyltransferase gene, is rare in the Chinese population. The present study focuses on a novel mutation with the Am phenotype in a Chinese individual.
Study design and methods
The sample with ABO blood group discrepancy was analyzed by serologic techniques. The full coding and flanking regions of the ABO gene,...
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