A weak blood group A phenotype caused by a new mutation at theABOlocus
Author:
Affiliation:
1. From the Department of Transfusion Medicine, Hannover Medical School, Hannover, Germany;
2. Biotest AG, Dreieich, Germany;
3. Institute of Transfusion Medicine, Charité, Campus Virchow‐Klinikum, Humboldt University, Berlin, Germany.
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1537-2995.2002.00046.x
Reference23 articles.
1. Molecular genetic basis of the histo-blood group ABO system
2. Genomic organization of human histo-blood group ABO genes
3. Genomic Cloning of the Human Histo-Blood Group ABO Locus
4. 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
5. Molecular Genetic Analysis of the ABO Blood Group System: 1. Weak Subgroups: A3and B3Alleles
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