# Functional FOXC1 variants in familial and sporadic atrial septal defect with cellular and animal validation

**Authors:** Huan‐Xin Chen, Hai‐Tao Hou, Xiu‐Li Wang, Jun Wang, Qin Yang, Guo‐Wei He

PMC · DOI: 10.1002/ctm2.1676 · Clinical and Translational Medicine · 2024-06-25

## Full-text entities

- **Genes:** FOXC1 (forkhead box C1) [NCBI Gene 2296] {aka ARA, ASGD3, FKHL7, FREAC-3, FREAC3, IGDA}
- **Diseases:** atrial septal defect (MESH:D006344)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11199059/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11199059/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC11199059/full.md

---
Source: https://tomesphere.com/paper/PMC11199059