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NewRHCEvariant alleles encoding the D- - phenotype

  • Published:2013-09-10 Issue: Volume: Page:n/a-n/a
  • ISSN:0041-1132
  • Container-title:Transfusion
  • language:en
  • Short-container-title:Transfusion

Author:

Ochoa-Garay Gorka1,Moulds Joann M.2,Cote Jacqueline3,Kresie Lesley4,Garaizar Adirane1,Goldman Mindy3,Wynn Polly4

Affiliation:

1. R&D Department; Progenika Inc.; Medford; Massachusetts

2. Scientific Support Services; LifeShare Blood Centers; Shreveport; Louisiana

3. National Immunohematology Reference Laboratory; Canadian Blood Services; Ottawa; Ontario; Canada

4. Immunohematology Reference Laboratory, Reference and Transfusion Services; Carter BloodCare; Tyler; Texas

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Reference23 articles.

1. Lack of RH C/E expression in the Rhesus D- phenotype is the result of a gene deletion;Blunt;Ann Hum Genet,1994

2. Nucleotide deletion in RHCE*cE (907delC) is responsible for a D- haplotype in Hispanics;Westhoff;Transfusion,2011

3. Rhnull syndrome: identification of a novel mutation in Rhce;Rosa;Transfusion,2005

4. Diversity of RHCE and identification of twelve new alleles;Vege;Transfusion,2010

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