Nondeletional ABO*O alleles frequently cause blood donor typing problems
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2005.00206.x/fullpdf
Reference15 articles.
1. Issitt PD Anstee DJ Applied blood group serology. Montgomery Scientific Publications; 188
2. Structural basis for the inactivity of human blood group O2 glycosyltransferase;Lee;J Biol Chem,2005
3. New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes;Hosseini-Maaf;Transfusion,2005
4. Nondeletional ABO*O alleles express weak blood group A phenotypes;Seltsam;Transfusion,2005
5. Systematic analysis of the ABO gene diversity within exons 6 and 7 by PCR-screening revealed new ABO alleles;Seltsam;Transfusion,2003
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1. Polymorphism of ABO*O alleles and its clinical significance;Oncohematology;2021-11-11
2. Lack of association between SNPsrs8176719 (O blood group) and COVID ‐19: Data from Spanish age matched patients and controls;Transfusion;2020-12
3. 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
4. Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABO*O.09.01 in Korea;Annals of Laboratory Medicine;2019-11-01
5. Molecular Genetic and Serologic Analysis of theOallele in the Korean Population;The Korean Journal of Blood Transfusion;2019-08-31
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