Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Amphenotype
Author:
Affiliation:
1. Department of Legal Medicine; Gunma University Graduate School of Medicine; Maebashi Japan
2. Japanese Red Cross Central Blood Institute; Tokyo Japan
3. Japanese Red Cross Kanto-Koshinetsu Block Blood Center; Tokyo Japan
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/vox.12077/fullpdf
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4. The ABO blood group gene: a locus of considerable genetic diversity;Chester;Transfus Med Rev,2001
5. Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes;Ogasawara;Immunogenetics,2001
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