A 24‐base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O-Reference-Cited by-同舟云学术

A 24‐base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O

Published:2020-06-04 Issue:7 Volume:60 Page:1564-1572
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Matzhold Eva Maria¹^ORCID,Drexler Camilla¹,Wagner Andrea¹,Bernecker Claudia¹,Pessentheiner Ariane²³,Bogner‐Strauß Juliane Gertrude²,Helmberg Wolfgang¹,Wagner Thomas¹

Affiliation:

1. Department of Blood Group Serology and Transfusion MedicineMedical University of Graz Graz Austria

2. Institute of BiochemistryTechnical University of Graz Graz Austria

3. Division of Endocrinology and MetabolismUniversity of California San Diego California USA

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15907

Reference43 articles.

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

4. The nature of diversity and diversification at the ABO locus

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