Associated Papers
Evidence for NR2F2/COUP-TFII involvement in human testis development.
Wankanit S et al.
Scientific Reports, 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
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children.
Bashamboo A et al.
American Journal of Human Genetics, 2018
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