Associated Papers
Role of COUP‑TFII in cardiovascular diseases and colorectal cancer: Insights into the molecular mechanisms and clinical relevance (Review).
Park TH et al.
Molecular Medicine Reports, 2025
Rare pathogenic NR2F2 (COUP-TFII) variants as potential etiological causes in pediatric patients with congenital heart diseases (CHDs).
Mansoor W et al.
Hellenic Journal of Cardiology : Hjc = Hellenike Kardiologike Epitheorese, 2025
Human Genetics of Ventricular Septal Defect.
Perrot A et al.
Advances in Experimental Medicine and Biology, 2024
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays.
Ganapathi M et al.
European Journal of Human Genetics : Ejhg, 2023
A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.
Qiao XH et al.
European Journal of Medical Genetics, 2018
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