The c.939G>A synonymous polymorphism in RHCE can be encountered on different molecular backgrounds-Reference-Cited by-同舟云学术

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The c.939G>A synonymous polymorphism in RHCE can be encountered on different molecular backgrounds

Published:2019-03-28 Issue: Volume: Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Filosa Lugdivine¹²³,Laget Laurine³,Chiaroni Jacques¹²³,Bailly Pascal¹²,Silvy Monique¹²

Affiliation:

1. Biologie des Groupes SanguinsÉtablissement Français du Sang PACA Corse Marseille France

2. Biologie des Groupes SanguinsAix Marseille University, CNRS, EFS, ADES Marseille France

3. Laboratoire d'Immuno‐Hématologie ReceveurÉtablissement Français du Sang PACA Corse Marseille France

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15266

Reference5 articles.

1. A silent mutation 939g>A in RHCE (Pro313) causes loss of a splice site and complete skipping of Exon 6 resulting in expression of novel E antigen;Green C;Transfus Med,2010

2. A comprehensive survey of both RHD and RHCE allele frequencies in sub‐Saharan Africa;Granier T;Transfusion,2013

3. Identification of six new RHCE variant alleles in individuals of diverse racial origin

4. Molecular basis of the JAHK (RH53) antigen

5. The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids

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