A novel ABCG2 variant causing Jr(a-) phenotype
- PMID: 38361420
- DOI: 10.1111/trf.17752
A novel ABCG2 variant causing Jr(a-) phenotype
Keywords: blood group genomics; immunohematology (RBC serology, blood groups).
References
REFERENCES
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- Zelinski T, Coghlan G, Liu XQ, Reid ME. ABCG2 null alleles define the Jr(a‐) blood group phenotype. Nat Genet. 2012;44(2):131–132. https://doi.org/10.1038/ng.1075
-
- Nakajima H, Ito K. An example of anti‐Jra causing hemolytic disease of the newborn and frequency of Jra antigen in the Japanese population. Vox Sang. 1978;35(4):265–267. https://doi.org/10.1111/j.1423-0410.1978.tb02932.x
-
- Kwon MY, Su L, Arndt PA, Garratty G, Blackall DP. Clinical significance of anti‐Jra: report of two cases and review of the literature. Transfusion. 2004;44(2):197–201. https://doi.org/10.1111/j.1537-2995.2004.00643.x
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- Kim MS, Kim JS, Park H, Chung Y, Kim H, Ko DH, et al. Fatal hemolytic disease of the fetus and newborn caused by anti‐Jra antibody: a case report and literature review. Transfus Apher Sci. 2020;59(1):102605. https://doi.org/10.1016/j.transci.2019.06.029
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