A novelABOO allele caused by a large deletion covering two exons of the ABO gene identified in a Caucasian family showing discrepant ABO blood typing results-Reference-Cited by-同舟云学术

A novelABOO allele caused by a large deletion covering two exons of the ABO gene identified in a Caucasian family showing discrepant ABO blood typing results

Published:2016-08-21 Issue:11 Volume:56 Page:2739-2743
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Matzhold Eva M.¹,Drexler Camilla¹,Wagner Thomas¹

Affiliation:

1. Department of Blood Group Serology and Transfusion Medicine; Medical University of Graz; Graz Austria

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.13768/fullpdf

Reference20 articles.

1. Molecular genetic basis of the histo-blood group ABO system;Yamamoto;Nature,1990

2. Antigen structure and genetic basis of histo-blood groups A, B and O: their changes associated with human cancer;Hakomori;Biochim Biophys Acta,1999

3. Glycosyltransferases. Structure, localization, and control of cell type-specific glycosylation;Paulson;J Biol Chem,1989

4. The membrane-binding domain of a rat liver Golgi sialyltransferase;Paulson;Biochem Soc Trans,1987

5. Systematic analysis of the ABO gene diversity within exons 6 and 7 by PCR screening reveals new ABO alleles;Seltsam;Transfusion,2003

Cited by 9 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. Allele‐specific long‐range sequencing as a method for ABO haplotyping in clinical blood group diagnosis and immunohematology research;Molecular Genetics & Genomic Medicine;2023-11-15

2. Identification of a novel c. 259G > T mutation in the ABO * B.01 allele giving rise to a B ₃ phenotype;Transfusion;2022-06-17

3. A 24‐base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O;Transfusion;2020-06-04

4. Genomic analysis of blood samples with serologicABOdiscrepancy identifies 12 novel alleles in a Chinese Han population;Transfusion Medicine;2020-05-25

5. Identification of a novel missense mutation c.29G>T in the ABO*A1.02 allele from a Chinese individual with an A subtype;Transfusion;2019-03-27