Serological weak D phenotype caused by a novel <scp> <i>RHD</i> </scp> variant allele with a nucleotide change (c. <scp>283G</scp> >T)
The authors have disclosed no conflicts of interest. Research data are not shared. TABLE S1. The primer sequences and their respective concentrations for TGS. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Authors
- Jue Hou (ORCID: https://orcid.org/0000-0003-3394-4625)
- M. Li
- Yuwei Zhao (ORCID: https://orcid.org/0000-0003-4351-7731)
- Xue Chen
Institutions
- Guangzhou Blood Center (CN)
- Shanghai Blood Center (CN)
Publication Details
- Journal
- Transfusion
- Published
- 2026-01-20
- DOI
- https://doi.org/10.1111/trf.70041
- Primary Topic
- Blood groups and transfusion
- Type
- article
- Field-Weighted Citation Impact
- 0.00