Genotyping confirms inheritance of the rare At(a−) type in a case of haemolytic disease of the newborn
Author:
Affiliation:
1. Research and Development, Australian Red Cross Blood Service QLD Australia
2. Red Cell Reference Laboratory, Australian Red Cross Blood Service QLD Australia
3. National Blood Centre, Thai Red Cross SocietyBangkok Thailand
Funder
Australian Red Cross Blood Service for the provision of blood products and services to the Australian community
Publisher
Wiley
Subject
Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjp2.33
Reference6 articles.
1. A Very Frequent Red Cell Antigen, Ata
2. Human Blood Groups
3. Anti-Ata causing mild hemolytic disease of the newborn
4. Severe delayed hemolytic transfusion reaction secondary to anti-Ata
5. Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization
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