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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| Huvudupphov: | , , |
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| Materialtyp: | Artigo |
| Språk: | Chinês |
| Utgiven: |
Institute of Blood Transfusion of Chinese Academy of Medical Sciences
2024-12-01
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| Serie: | Zhongguo shuxue zazhi |
| Ämnen: | |
| Länkar: | https://www.cjbt.cn/thesisDetails#10.13303/j.cjbt.issn.1004-549x.2024.12.014&lang=en |
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