Identification of a novel <scp><i>B</i></scp> allele with a c.<scp>145C</scp>>T variant-Reference-Cited by-同舟云学术

Identification of a novel B allele with a c.145C>T variant

Published:2023-06-22 Issue:8 Volume:63 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Fan Cuihua¹²^ORCID,Yang Xiaojun³^ORCID,Su Yanping¹²,Zhang Jiandong⁴⁵,Chen Fawen³,Qiu Dongbiao¹²

Affiliation:

1. Department of Blood Transfusion The First Affiliated Hospital of Fujian Medical University Fuzhou Fujian China

2. Department of Blood Transfusion National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University Fuzhou Fujian China

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

4. The Center of Information The First Affiliated Hospital of Fujian Medical University Fuzhou Fujian China

5. The Center of Information National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University 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.17401

Reference5 articles.

1. Missense mutations outside the catalytic domain of the ABO glycosyltransferase can cause weak blood group A and B phenotypes

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

3. Human blood group glycosyltransferases. I. Purification of n-acetylgalactosaminyltransferase.

4. Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bmsubgroup individual

5. A novel Bweak hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels