c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype
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DOI: 10.1111/trf.16890
Abstract: ABO subgroups result from ABO gene variants which brings about the ABO typing discrepancy. ABO*A1.01 allele is used as a reference for the sequences of all other ABO alleles. Many of the A suballeles contain… read more here.
Keywords: 586t mutation; abo; ael phenotype; abo allele ... See more keywords