Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype

Y. Takahashi, K. Isa, R. Sano, T. Nakajima, R. Kubo, K. Takahashi, Y. Kominato, H. Tsuneyama, K.  Ogasawara and & M. Uchikawa 

Vox Sang 2014 106, 167 – 175