Identification of a novel A allele with a c.731T>C mutation on the ABO * A1 .02 allele
Author:
Affiliation:
1. Transfusion Research Institute, Blood Center of Zhejiang Province Hangzhou China
2. Zhejiang Provincial Key Laboratory of Blood Safety Research Hangzhou China
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15902
Reference5 articles.
1. Hemolysis from ABO Incompatibility
2. Current state of transfusion practices for ABO-incompatible pediatric heart transplant patients in the United States and Canada
3. A novel mutation +5904 C>T of RUNX1 site in the erythroid cell-specific regulatory element decreases the ABO antigen expression in Chinese population
4. Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene
5. c.830T>C mutation on the ABO*A1.02 allele responsible for Aw phenotype
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1. Identification of a novel ABO*A1.02 allele with variant c. 671T >C;Transfusion;2022-12-13
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