c.830T>C mutation on the ABO*A1.02 allele responsible for Aw phenotype
Author:
Affiliation:
1. Blood Center of Zhejiang ProvinceTransfusion Research Institute Hangzhou China
2. Zhejiang Provincial Key Laboratory of Blood Safety Research Hangzhou China
Funder
Research Foundation of Zhejiang Province
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15413
Reference5 articles.
1. ABO Research in the Modern Era of Genomics
2. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project
3. Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene
4. Distribution of ABO blood group allele and identification of three novel alleles in the Chinese Han population
5. A novel mutation +5904 C>T of RUNX1 site in the erythroid cell-specific regulatory element decreases the ABO antigen expression in Chinese population
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Analysis of the Genomic Sequence of ABO Allele Using Next-Generation Sequencing Method;Frontiers in Immunology;2022-07-06
2. Identification of a novel A allele with a c.731T>C mutation on the ABO * A1 .02 allele;Transfusion;2020-07-03
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