c.586T>C mutation on the ABO*A1.02 allele responsible for A_el phenotype

Transfusion. 2022 Jun;62(6):E27-E29. doi: 10.1111/trf.16890. Epub 2022 Apr 26.

Authors

Yuqing Shen¹, Xiaojun Yang², Chunjing Lu¹, Fawen Chen², Xianren Ye³, Naizhu Su¹

Affiliations

¹ Department of Transfusion, Women and Children's Hospital, School of Medicine, Xiamen University, Xiamen, Fujian, China.
² Department of Transfusion, Fujian Provincial Hospital, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, Fujian, China.
³ Department of Transfusion, Fujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, Fujian, China.

PMID: 35470871
DOI: 10.1111/trf.16890

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

ABO Blood-Group System* / genetics
Alleles
Genotype
Humans
Mutation
Phenotype

Substances

ABO Blood-Group System