Identification of a novel A allele with a c.731T>C mutation on the ABO*A1.02 allele
- PMID: 32619045
- DOI: 10.1111/trf.15902
Identification of a novel A allele with a c.731T>C mutation on the ABO*A1.02 allele
References
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- Ying Y, Chen S, Ma K, et al. Identification of a novel B allele with missense mutation (c.98G>C) in the ABO gene. Transfusion 2017;57:219-20.
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- Hong X, Chen S, Ma K, et al. c.830T>C mutation on the ABO*A1.02 allele responsible for Aw phenotype. Transfusion 2019;59:E11-2.
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