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Article

Weak D antigen expression caused by a novel RHD allele in Argentineans.

Transfusion - 1 Nov 2016

Trucco Boggione Carolina, Luján Brajovich Melina Eliana, Gaspardi Ane Caroline, Sippert Emilia, Mattaloni Stella Maris, Leri Mónica, Biondi Claudia, Castilho Lilian, Cotorruelo Carlos Miguel

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27611815
DOI: 10.1111/trf.13790

Genes

RHD

Provenance

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Related research

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Weak D antigen expression caused by a novel RHD allele in Argentineans.PMID 27611815Read ↗

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Reduced RhD antigen expression caused by two novel RHD variant alleles.Semantic proximity Read ↗

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[Serological and molecular study of RHD weak D expression mutant--a case report].Semantic proximity Read ↗

The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype.Semantic proximity Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

Molecular characterization of 13 new RHD alleles.Semantic proximity Read ↗

Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.Semantic proximity Read ↗

A novel RHCE*03 with 255G > A, 538G > A, and Exon 9 of RHD in a Chinese individual encodes for altered c and E antigens.Semantic proximity Read ↗

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