c.586T>C mutation on the <i>ABO*A1.02</i> allele responsible for A <sub>el</sub> phenotype-Reference-Cited by-同舟云学术

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c.586T>C mutation on the ABO*A1.02 allele responsible for A _el phenotype

Published:2022-04-26 Issue:6 Volume:62 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Shen Yuqing¹,Yang Xiaojun²^ORCID,Lu Chunjing¹,Chen Fawen²,Ye Xianren³,Su Naizhu¹

Affiliation:

1. Department of Transfusion Women and Children's Hospital, School of Medicine, Xiamen University Xiamen Fujian China

2. Department of Transfusion Fujian Provincial Hospital, Shengli Clinical Medical College of Fujian Medical University Fuzhou Fujian China

3. Department of Transfusion Fujian Medical University Cancer Hospital, Fujian Cancer Hospital Fuzhou Fujian China

Funder

Fujian Provincial Health Technology Project

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16890

Reference5 articles.

1. Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles

2. Molecular Basis of ABO Variants Including Identification of 16 Novel ABO Subgroup Alleles in Chinese Han Population

3. c.543G>C mutation in ABO*A.1.02 allele responsible for a weak A phenotype

4. Many genetically defined ABO subgroups exhibit characteristic flow cytometric patterns

5. Identification of novel variant B alleles within the ABO gene

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