Five novel <i>ZNF469</i> gene mutations in sporadic keratoconus patients in the Han Chinese population.
Mutations in the <i>ZNF469</i> gene may contribute to the development of KC in the Han Chinese population. These mutation sites may provide valuable information for future genetic screening of KC patients and their families.
Authors
- Feng Su (ORCID: https://orcid.org/0000-0002-0509-6764)
- Feng Zhang (ORCID: https://orcid.org/0000-0002-1371-266X)
- Guiyun He
- Xiao Li (ORCID: https://orcid.org/0000-0002-9411-3414)
- Yanna Cao (ORCID: https://orcid.org/0000-0002-5639-1675)
- Zhihong Deng (ORCID: https://orcid.org/0000-0002-3738-8147)
Institutions
- Central South University (CN)
- Hunan Normal University (CN)
- Third Xiangya Hospital (CN)
- Xiangya Hospital Central South University (CN)
Publication Details
- Journal
- PubMed
- Published
- 2025-06-28
- DOI
- https://doi.org/10.11817/j.issn.1672-7347.2025.240114
- Primary Topic
- Corneal surgery and disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00