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
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
Novel de novo pathogenic variant in the NR2F2 gene in a boy with congenital heart defect and dysmorphic features.
Upadia J et al.
American Journal of Medical Genetics. Part A, 2018
Rare variants in NR2F2 cause congenital heart defects in humans.
Al Turki S et al.
American Journal of Human Genetics, 2014
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