Novel ABO gene variants caused by missense mutations in Exon 7 leading to discrepant ABO blood typing results
Author:
Affiliation:
1. Department of Blood Group Serology and Transfusion Medicine; Medical University of Graz; Graz Austria
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.13025/fullpdf
Reference5 articles.
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2. The nature of diversity and diversification at the ABO locus;Seltsam;Blood,2003
3. Genomic cloning of the human histo-blood group ABO locus;Bennett;Biochem Biophys Res Commun,1995
4. BGMUT: NCBI dbRBC database of allelic variations of genes encoding antigens of blood group systems;Patnaik;Nucleic Acids Res,2012
5. Human histo-blood group A2 transferase coded by A2 allele, one of the A subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal;Yamamoto;Biochem Biophys Res Commun,1992
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2. A 24‐base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O;Transfusion;2020-06-04
3. A novel cis-AB allele with c.797 T>C mutation identified in three unrelated Chinese individuals;Transfusion;2018-09-10
4. Genetic control of erythropoiesis;Current Opinion in Hematology;2017-05
5. A novelABOO allele caused by a large deletion covering two exons of the ABO gene identified in a Caucasian family showing discrepant ABO blood typing results;Transfusion;2016-08-21
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