c.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype
Author:
Affiliation:
1. Transfusion Medicine Research Institute, Blood Center of Zhejiang Province Hangzhou China
2. Key Laboratory of Blood Safety Research of Zhejiang Province Hangzhou China
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15496
Reference5 articles.
1. Protein stability changes of the novel p.Arg180Cys mutant A glycosyltransferase resulted in a weak A phenotype
2. The A312 allele (c.280A>T) is responsible for the weak A phenotype;Chun S;Ann Clin Lab Sci,2017
3. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project
4. Distribution of ABO blood group allele and identification of three novel alleles in the Chinese Han population
5. Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles;Cai X;Transfusion,2013
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1. One novel single nucleotide polymorphism c.424A>G on A1.02 allele in ABO glycosyltransferases leads to Aweak phenotype;Journal of the Formosan Medical Association;2024-02
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