WES and Transcriptome Analysis Identifies FN1 as a Candidate Gene for Anterior Segment Dysgenesis
This study identified an FN1 mutation associated with ASD patients and probed potential pathways related to it.
Authors
- Qinghong Lin
- Xiaosong Han (ORCID: https://orcid.org/0000-0002-6999-5419)
- Yan Wang (ORCID: https://orcid.org/0000-0002-1047-6075)
- Xiaoyu Zhang (ORCID: https://orcid.org/0000-0003-2820-6353)
- Xuejun Wang (ORCID: https://orcid.org/0000-0002-7034-0460)
- Xingtao Zhou (ORCID: https://orcid.org/0000-0003-4943-7740)
- Xiaoliao Peng
- Tian Han (ORCID: https://orcid.org/0000-0003-3867-9373)
- Ling Sun (ORCID: https://orcid.org/0000-0002-7061-7909)
- Yuwen Ran
Institutions
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Fudan University (CN)
- Eye & ENT Hospital of Fudan University (CN)
- He Eye Hospital (CN)
- Shanghai Clinical Research Center (CN)
Publication Details
- Journal
- The Journal of Gene Medicine
- Published
- 2024-11-27
- DOI
- https://doi.org/10.1002/jgm.70001
- Citations
- 1
- Primary Topic
- Intraocular Surgery and Lenses
- Type
- article
- Field-Weighted Citation Impact
- 0.54
Funders
- National Natural Science Foundation of China
- National Outstanding Youth Science Fund Project of National Natural Science Foundation of China
- National Postdoctoral Program for Innovative Talents