A novel O allele in the ABO blood group system, a nine‐base‐pair deletion in an ABO*O.01.01 allele
Author:
Affiliation:
1. Qingdao Blood Center Institute of Transfusion Medicine, The Affiliated Hospital of Qingdao University Qingdao China
2. Department of Blood Transfusion The Affiliated Hospital of Qingdao University Qingdao China
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16108
Reference5 articles.
1. ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies
2. Thorough analysis of unorthodoxABOdeletions called by the 1000 Genomes project
3. Expression of ABO blood-group genes is dependent upon an erythroid cell–specific regulatory element that is deleted in persons with the Bm phenotype
4. Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bmsubgroup individual
5. A novel A allele with c.689G>T mutation identified in a Chinese individual
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1. Identification of a novel A allele with a nucleotide insert (c.99‐1_100 T) in the ABO gene associated with a A3 phenotype individual;Transfusion;2023-09-04
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