A novel <i>RHD</i> allele caused by the <i>RHD IVS4</i> + <i>2delT</i> mutation identified in a Chinese Han male donor with a D‐negative phenotype
The authors have disclosed no conflicts of interest. The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.
Authors
- Xiao Hao (ORCID: https://orcid.org/0000-0002-5727-8666)
- Jie Li (ORCID: https://orcid.org/0000-0001-9915-5851)
- Ruirui Li
- Lu Zhang
Institutions
- Jinan Maternity And Care Hospital (CN)
- Guangzhou Blood Center (CN)
Publication Details
- Journal
- Transfusion
- Published
- 2026-03-07
- DOI
- https://doi.org/10.1111/trf.70136
- Primary Topic
- Blood groups and transfusion
- Type
- article
- Field-Weighted Citation Impact
- 0.00