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Article

Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency.

Nature genetics - 1 Feb 1996

Cherif-Zahar B, Raynal V, Gane P, Mattei M G, Bailly P, Gibbs B, Colin Y, Cartron J P

Abstract excerpt

The Rh antigen is a multi-subunit complex composed of Rh polypeptides and associated glycoproteins (Rh50, CD47, LW and glycophorin B); these interact in the red cell membrane and are lacking or severely reduced in Rhnull cells. As a result, individuals with Rhnull suffer chronic haemolytic anaemia known as the Rh-deficiency syndrome. Most frequently, Rhnull phenotypes are caused by homozygosity of an autosomal...

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Source

Identifiers

PMID: 8563755
DOI: 10.1038/ng0296-168

Genes

CD47

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.Semantic proximity Read ↗

Structure and expression of the RH locus in the Rh-deficiency syndrome.Semantic proximity Read ↗

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A splicing mutation of the RHAG gene associated with the Rhnull phenotype.Semantic proximity Read ↗

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