Exploration of the Pathogenic Mechanism of the Factor <scp>XIII</scp> A Subunit in a Patient With Congenital Factor <scp>XIII</scp> Deficiency
These findings provide valuable data accumulation that can contribute to the prevention of congenital FXIII deficiency, the exploration of potential pathogenic mechanisms, and the enrichment of genetic mutation databases.
Authors
- Chenglin Zhu (ORCID: https://orcid.org/0000-0003-3486-1936)
- Yinghui Zhao (ORCID: https://orcid.org/0000-0003-1105-8980)
- M Wang
- Lijun Qu (ORCID: https://orcid.org/0000-0002-7519-3121)
- Lijuan Zhu (ORCID: https://orcid.org/0000-0003-3531-3624)
- Hongjun Liu (ORCID: https://orcid.org/0000-0002-7508-8524)
- Tianping Chen
- Aoshuang Jiang
- Nan Wei
Institutions
- Anhui Provincial Hospital (CN)
- Anhui Provincial Children's Hospital (CN)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2026-01-01
- DOI
- https://doi.org/10.1002/mgg3.70193
- Primary Topic
- Blood properties and coagulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Anhui Medical University
- Natural Science Foundation of Anhui Province