ABO alleles are linked with haplotypes of an erythroid cell-specific regulatory element in intron 1 with a few exceptions attributable to genetic recombination

Author:

Nakajima T.1,Sano R.1,Takahashi Y.1,Watanabe K.1,Kubo R.1,Kobayashi M.1,Takahashi K.1,Takeshita H.2,Kominato Y.1

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

Publisher

Wiley

Subject

Hematology,General Medicine

Reference10 articles.

1. Geoff Daniels: Human Blood Groups 3rd edn West Sussex, UK Wiley-Blackwell 2013

2. http://www.ncbi.nlm.nih.gov/projects/gv/rbc/xslcgi.fcgi?cmd=bgmut/systems_info&system=abo

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. Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype;Takahashi;Vox Sang,2014

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