Identification of mutations associated with congenital cataracts in nineteen Chinese families
Our research findings have revealed multiple gene variants associated with cataracts, providing clinical guidance for improved molecular diagnosis of congenital cataracts in the era of precision medicine.
Authors
- Shen-Rong Zhang
- Mingcheng Wang (ORCID: https://orcid.org/0000-0002-3631-9174)
- Jialin Xu (ORCID: https://orcid.org/0000-0002-2456-3567)
- Kaiyi Zhu (ORCID: https://orcid.org/0000-0002-0111-0848)
- Yitong Xu
- Hai-Sen Sun
- Xiu‐Feng Huang (ORCID: https://orcid.org/0000-0002-7852-6358)
- Yaqi Wang (ORCID: https://orcid.org/0000-0002-7261-4947)
- Jin Li (ORCID: https://orcid.org/0000-0001-9201-2321)
- Wenkai Huang
- Zerun Liu (ORCID: https://orcid.org/0009-0005-5718-5952)
- Teng Huang
Institutions
- Wenzhou Medical University (CN)
- Affiliated Eye Hospital of Wenzhou Medical College (CN)
- Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University (CN)
Publication Details
- Journal
- BMC Ophthalmology
- Published
- 2025-02-24
- DOI
- https://doi.org/10.1186/s12886-025-03920-4
- Citations
- 2
- Primary Topic
- Connexins and lens biology
- Type
- article
- Field-Weighted Citation Impact
- 1.61
Funders
- National Natural Science Foundation of China