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- W2013553932 abstract "The A m and B m phenotypes are characterized by weak expression of the A or B antigens, respectively, by red blood cells with a normal expression by the saliva of secretors. Deletion of the regulatory element in the first intron of the ABO gene and disruption of the GATA motif in the element were found to be responsible. In this study, we identified a novel mutation within the GATA motif (G>C substitution at position c.28 + 5830) in the regulatory element of the A allele that might diminish transcription activity causing the generation of the A m B phenotype." @default.
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- W2013553932 date "2014-12-30" @default.
- W2013553932 modified "2023-10-17" @default.
- W2013553932 title "A novel mutation of the <scp>GATA</scp> site in the erythroid cell‐specific regulatory element of the <i><scp>ABO</scp></i> gene in a blood donor with the A<sub>m</sub>B phenotype" @default.
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- W2013553932 doi "https://doi.org/10.1111/vox.12229" @default.
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