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Two distinct RHCE alleles in cis to weak D type 31 alleles in individuals from different ethnicities.

作者信息

Srivastava Kshitij, Körmöczi Günther F, Joshi Sanmukh R, Flegel Willy A

机构信息

Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, Maryland.

Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, Austria.

出版信息

Transfusion. 2018 Oct;58(10):2465-2466. doi: 10.1111/trf.14929. Epub 2018 Sep 24.

Abstract
摘要

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It's time to phase out "serologic weak D phenotype" and resolve D types with RHD genotyping including weak D type 4.
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本文引用的文献

1
Serologic and molecular characterization of weak D type 29.
Transfusion. 2017 Oct;57(10):2542-2544. doi: 10.1111/trf.14218. Epub 2017 Jul 3.
2
Allo- and autoanti-D in weak D types and in partial D.
Transfusion. 2012 Sep;52(9):2067-9; author reply 2070. doi: 10.1111/j.1537-2995.2012.03693.x.
3
IVS5-38del4 deletion in the RHD gene does not cause a DEL phenotype: relevance for RHD alleles including DFR-3.
Transfusion. 2007 Aug;47(8):1552-5. doi: 10.1111/j.1537-2995.2007.01353.x.

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