[Identification and analysis of a novel RHCE allele underlying a RhD-- phenotype].
Above results revealed the molecular biological mechanism of a RhD-- phenotype. The c.365C>A variant in the RHCE gene has rendered the RHCE*cE alleles invalid, which ultimately led to the RhD-- phenotype.
Authors
- Ying Xie
- Yongkui Kong (ORCID: https://orcid.org/0000-0003-3583-4606)
- Qiankun Yang (ORCID: https://orcid.org/0000-0003-2850-6065)
- Yuxiang Lin (ORCID: https://orcid.org/0000-0002-3963-3468)
- Yanli Chang (ORCID: https://orcid.org/0000-0002-7940-9882)
- Hecai Yang
- Shuya Wang (ORCID: https://orcid.org/0000-0002-9360-9194)
- Xue Liu (ORCID: https://orcid.org/0000-0002-5159-8503)
- Li Wang (ORCID: https://orcid.org/0000-0003-2068-7535)
Institutions
- First Affiliated Hospital of Zhengzhou University (CN)
Publication Details
- Journal
- PubMed
- Published
- 2025-08-10
- DOI
- https://doi.org/10.3760/cma.j.cn511374-20240926-00508
- Primary Topic
- Blood groups and transfusion
- Type
- article
- Field-Weighted Citation Impact
- 0.00