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Article

Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population.

Transfusion - 1 Aug 2013

Ye Luyi, He Yunlei, Gao Huanhuan, Guo Zhonghui, Zhu Ziyan

Abstract excerpt

BACKGROUND: Although more than 80 weak D types have been reported, many rare alleles probably remain unidentified. However, direct evidence that associates intronic mutations in the RHD gene with weak D types is lacking. STUDY DESIGN AND METHODS: Blood samples were obtained from Shanghai Blood Center. D- samples typed in routine laboratories were tested using a monoclonal immunoglobulin M reagent, an indirect...

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PMID: 23216299
DOI: 10.1111/trf.12002

Genes

RHD

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