A novel variant DO*A allele with a c.370delT mutation leading to a DO ‐null phenotype in a Syrian family-Reference-Cited by-同舟云学术

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A novel variant DO*A allele with a c.370delT mutation leading to a DO ‐null phenotype in a Syrian family

Published:2020-11-18 Issue:2 Volume:61 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Morin Pierre‐Aurèle¹^ORCID,Ethier Carole²,Lavoie Josée³,Robitaille Nancy⁴,Baillargeon Nadia²^ORCID

Affiliation:

1. Department of Medicine, Faculty of Medicine and Health Sciences Université de Sherbrooke Sherbrooke Quebec Canada

2. Immunohematology Reference Laboratory Héma‐Québec Québec City Quebec Canada

3. Division of Medical Affairs and Innovation Héma‐Québec Québec City Quebec Canada

4. Division of Transfusion Medicine Héma‐Québec Montréal Quebec Canada

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16193

Reference5 articles.

1. Complexities of the Dombrock blood group system revealed

2. International Society of Blood Transfusion (ISBT). Red cell immunogenetics and blood group terminology. DO (ISBT 014) blood group alleles v4.1 [Internet]. Amsterdam: ISBT Central Office; c2020 [cited 2020 August 20].http://www.isbtweb.org/working-parties/redcell-immunogenetics-and-blood-group-terminology/

3. Serological and molecular characterization of DOLC, a novel high incidence antigen in the Dombrock blood group system [abstract];Karamatic Crew V;Vox Sang,2013

4. A Dombrock system antibody detects a new high‐prevalence antigen, DODE;Shakarian G;Transfusion,2015

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