A novel <scp> <i>RHD</i> </scp> variant allele harboring c.487‐ <scp>14G</scp> >A in trans to an <scp> <i>RHD</i> </scp> ‐null allele associated with reduced <scp> <i>RHD</i> </scp> expression
The authors declare no conflicts of interest. The data that support the findings of this study are openly available in GenBank under accession number PQ801658.1. The GenBank record has been updated to annotate NM_016124.6(RHD):c.487-14G>A.
Authors
- Jia Zhang (ORCID: https://orcid.org/0000-0002-4819-177X)
- Xi Yuan (ORCID: https://orcid.org/0000-0002-1865-530X)
- Qunjuan Zeng
- Yulin Qian
- Xin Jiao
Institutions
- Dazhou Central Hospital (CN)
Publication Details
- Journal
- Transfusion
- Published
- 2026-08-17
- DOI
- https://doi.org/10.1111/trf.70370
- Primary Topic
- Blood disorders and treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00