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Article

The R0Har RH:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene.

British journal of haematology - 1 Mar 1996

Beckers E A, Faas B H, von dem Borne A E, Overbeeke M A, van Rhenen D J, van der Schoot C E

Abstract excerpt

The highly polymorphic Rh (Rhesus) system is encoded by two homologous genes, one encoding the D polypeptide and the other the CcEe polypeptides. Partial D antigens may be caused by gene rearrangements, deletions or point mutations. In this study the molecular basis of R0Har RH:33, a Rh phenotype...

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Source

Identifiers

PMID: 8616049
DOI: 10.1046/j.1365-2141.1996.382918.x

Genes

RHD
RHCE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-8616049-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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The R0Har RH:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene.PMID 8616049Read ↗

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