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Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression.

Transfusion - 1 Apr 2023

Vege Sunitha, Floch Aline, Burgos Anna, Tahiri Toufik, Kirkegaard Julie, Dupont Megan, Ochoa-Garay Gorka, Lomas-Francis Christine, Westhoff Connie M

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PMID: 36722377
DOI: 10.1111/trf.17256

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Related research

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Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression.PMID 36722377Read ↗

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Molecular analysis of selected Rh variants.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 ↗

A Novel RHCE*cE (c.827C>A) Allele, Containing the Single-Nucleotide Change, Encodes Altered c/E Antigens.Semantic proximity Read ↗

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

A novel RHCE*cE allele identified in a Chinese individual, encodes weakened expression of c and E antigens.Semantic proximity Read ↗

Identification of a novel RHCE*Ce (829G > A) allele associated with absence of C and e antigens expression.Semantic proximity Read ↗

The Analysis of Nucleotide Substitutions, Gaps, and Recombination Events between RHD and RHCE Genes through Complete SequencingSemantic proximity Read ↗

The low prevalence Rh antigen Be(a) (Rh36) is associated with RHCE*ce 662C>G in exon 5, which is predicted to encode Rhce 221Arg.Semantic proximity Read ↗

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