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Deletion of the regulatory element in the first intron of the<jats:italic><jats:styled-content style=\"fixed-case\">ABO<\/jats:styled-content><\/jats:italic>gene and disruption of the<jats:styled-content style=\"fixed-case\">GATA<\/jats:styled-content>motif in the element were found to be responsible. In this study, we identified a novel mutation within the<jats:styled-content style=\"fixed-case\">GATA<\/jats:styled-content>motif (G&gt;C substitution at position c.28\u00a0+\u00a05830) in the regulatory element of the<jats:italic>A<\/jats:italic>allele that might diminish transcription activity causing the generation of the A<jats:sub>m<\/jats:sub>B phenotype.<\/jats:p>","DOI":"10.1111\/vox.12229","type":"journal-article","created":{"date-parts":[[2014,12,30]],"date-time":"2014-12-30T15:34:00Z","timestamp":1419953640000},"page":"425-427","source":"Crossref","is-referenced-by-count":19,"title":["A novel mutation of the<scp>GATA<\/scp>site in the erythroid cell\u2010specific regulatory element of the<i><scp>ABO<\/scp><\/i>gene in a blood donor with the A<sub>m<\/sub>B phenotype"],"prefix":"10.1111","volume":"108","author":[{"given":"A.","family":"Oda","sequence":"first","affiliation":[{"name":"Japanese Red Cross Kinki Block Blood Center Osaka 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