Structural and functional assessment of TBX20 gene variants in pediatric ventricular septal defect
The findings underscore the involvement of TBX20 gene variants in the etiology of pediatric VSD and provide mechanistic insights that may inform future clinical research and the development of targeted therapeutic strategies.
Authors
- Jie Wang (ORCID: https://orcid.org/0000-0002-1399-7079)
- Yanmei Jin (ORCID: https://orcid.org/0000-0003-2067-4347)
- Zhenzhen Qin (ORCID: https://orcid.org/0000-0002-5266-5691)
- Caixia Liu (ORCID: https://orcid.org/0000-0001-5851-6374)
Institutions
- Meizhou City People's Hospital (CN)
- Shanxi Provincial Children's Hospital (CN)
Publication Details
- Journal
- Hereditas
- Published
- 2025-08-04
- DOI
- https://doi.org/10.1186/s41065-025-00513-5
- Primary Topic
- Congenital Heart Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Chinese Academy of Sciences
- Natural Science Foundation of Shanxi Province