A variant RhAG protein encoded by theRHAG*572Aallele causes serological weak D expression while maintaining normal RhCE phenotypes-Reference-Cited by-同舟云学术

A variant RhAG protein encoded by theRHAG*572Aallele causes serological weak D expression while maintaining normal RhCE phenotypes

Published:2018-10-04 Issue:1 Volume:59 Page:405-411
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Wen Jizhi¹,Verhagen Onno J.H.M.²,Jia Shuangshuang¹,Liang Qianni³,Wang Zhen¹,Wei Ling¹,Luo Hong¹,Luo Guangping¹,Vidarsson Gestur²,Akker Emile²,Ji Yanli¹,Schoot C. Ellen²

Affiliation:

1. Institute of Clinical Blood Transfusion, Guangzhou Blood Center Guangzhou People's Republic of China

2. Sanquin Research and Landsteiner Laboratory, Academic Medical CentreUniversity of Amsterdam Amsterdam The Netherlands

3. Department of Blood TransfusionGuangdong No. 2 Provincial People's Hospital Guangzhou People's Republic of China

Funder

Science and Technology Project of Guangzhou City

Key Medical Disciplines and Specialties Program of Guangzhou

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.14969

Reference29 articles.

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2. Unexpected red blood cell antibody distributions in Chinese people by a systematic literature review

3. Molecular basis of weak D phenotypes;Wagner FF;Blood,1999

4. Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using theRHDgenotype

5. The Rhesus Site

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