Genetic analysis of a serologically weak D phenotype caused by the p. R191G variant of the RHAG gene

[Objective] To analyze the molecular mechanism of a serologically weak D phenotype caused by RHAG gene variation. [Methods] The full coding and flanking regions of RHD, RHCE and RHAG genes of the serologically weak D phenotype sample were identified through direct sequencing. Bioinformatics software...

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Päätekijät:	ZHANG Xu, LI Xiaofeng, LI Jianping
Aineistotyyppi:	Artigo
Kieli:	Chinês
Julkaistu:	Institute of Blood Transfusion of Chinese Academy of Medical Sciences 2024-12-01
Sarja:	Zhongguo shuxue zazhi
Aiheet:	serologically weak d phenotype rhd gene rhag gene bioinformatics analysis
Linkit:	https://www.cjbt.cn/thesisDetails#10.13303/j.cjbt.issn.1004-549x.2024.12.014&lang=en
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