Deletion of the RUNX1 binding site in the erythroid cell‐specific regulatory element of the ABO gene in two individuals with the Am phenotype
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M. Uchikawa | K. Ogasawara | H. Tsuneyama | R. Sano | R. Kubo | Y. Kominato | K. Isa | T. Nakajima | Y. Takahashi | K. Takahashi