Presence of nucleotide substitutions in theABOpromoter in individuals with phenotypes A3and B3

Author:

Isa K.1,Yamamuro Y.1,Ogasawara K.1,Yabe R.2,Ogiyama Y.3,Ito S.3,Takahashi Y.4,Kominato Y.4,Sano R.4,Uchikawa M.2

Affiliation:

1. Japanese Red Cross Central Blood Institute; Tokyo Japan

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

3. Japanese Red Cross Touhoku Block Blood Center; Sendai Japan

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

Publisher

Wiley

Subject

Hematology,General Medicine

Reference9 articles.

1. Human Blood Groups

2. Molecular genetics of ABO;Yamamoto;Vox Sang,2000

3. Expression of ABO blood-group genes is dependent upon an erythroid cell-specific regulatory element, which is deleted in persons with the Bm phenotype;Sano;Blood,2012

4. Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual;Nakajima;Transfusion,2013

5. Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles;Cai;Transfusion,2013

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