Identification of a novel frequentRHCE*ce308Tvariant allele in Chinese D– individuals, resulting in a C+c

Identification of a novel frequentRHCE*ce308Tvariant allele in Chinese D– individuals, resulting in a C+c– phenotype

Published:2016-06-24 Issue:9 Volume:56 Page:2314-2321
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Stegmann Tamara C.¹,Ji Yanli²,Bijman Renate¹,Wang Zhen²,Wen Jizhi²,Wei Ling²,Veldhuisen Barbera¹,Haer‐Wigman Lonneke¹,Lighthart Peter³,Lodén‐van Straaten Martin⁴,Luo Guangping²,van der Schoot C. Ellen¹

Affiliation:

1. Sanquin Research and Landsteiner LaboratoryAcademic Medical Centre, University of AmsterdamAmsterdam The Netherlands

2. Institute of Clinical Blood Transfusion, Guangzhou Blood CenterGuangzhou China; and

3. MRC‐Holland b.vAmsterdam The Netherlands

4. Sanquin Diagnostic ServicesAmsterdam The Netherlands

Funder

National Natural Science Foundation of China

Science and Technology Project of Guangzhou City

Key Medical Disciplines and Specialties Program of Guangzhou in China

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.13709

Reference33 articles.

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4. Sequence Analysis of cDNA Derived from Reticulocyte mRNAs Coding for Rh Polypeptides and Demonstration of E/e and C/c Polymorphisms

5. Evidence supporting the requirement for two proline residues for expression of c

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