Identification of an <scp>A<sub>weak</sub>B</scp> phenotype caused by significant <scp>ABO</scp> gene deletion in a Chinese woman
We report for the first time that large fragment deletions represent a novel molecular basis for the A<sub>weak</sub>B. These deletions may potentially influence the expression of the A antigen.
Authors
- Zhiwei Liu
- Feiyu Jiang (ORCID: https://orcid.org/0000-0002-3583-1096)
- Shoufang Xu
- Xinhui Wang (ORCID: https://orcid.org/0000-0001-7713-6262)
- Yingying Zhang
- Weiwei Zheng (ORCID: https://orcid.org/0000-0003-0806-2997)
- Tian Gao (ORCID: https://orcid.org/0009-0001-3563-4017)
Institutions
- Sir Run Run Shaw Hospital (CN)
- Zhejiang University (CN)
Publication Details
- Journal
- Vox Sanguinis
- Published
- 2025-03-12
- DOI
- https://doi.org/10.1111/vox.70008
- Primary Topic
- Blood groups and transfusion
- Type
- article
- Field-Weighted Citation Impact
- 0.00