A 3·0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bmphenotype

Author:

Sano R.1,Kuboya E.1,Nakajima T.1,Takahashi Y.1,Takahashi K.1,Kubo R.1,Kominato Y.1,Takeshita H.2,Yamao H.3,Kishida T.4,Isa K.5,Ogasawara K.5,Uchikawa M.6

Affiliation:

1. Department of Legal Medicine; Gunma University Graduate School of Medicine; Maebashi Japan

2. Department of Legal Medicine; Shimane University School of Medicine; Izumo Japan

3. Inoue Hospital; Nobeoka Japan

4. Department of Legal Medicine; Oita University; Yuhu Japan

5. Japanese Red Cross Central Blood Institute; Tokyo Japan

6. Japanese Red Cross Kanto-Koshinetsu Block Blood Center; Tokyo Japan

Publisher

Wiley

Subject

Hematology,General Medicine

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