Rare variants in NR2F2 cause congenital heart defects in humans. by Al Turki, S, Manickaraj, A, Mercer, C, Gerety, S, Hitz, M, Lindsay, S, D'Alessandro, L, Swaminathan, G, Bentham, J, Arndt, A, Low, J, Breckpot, J, Gewillig, M, Thienpont, B, Abdul-Khaliq, H, Harnack, C, Hoff, K, Kramer, H, Schubert, S, Siebert, R, Toka, O, Cosgrove, C, Watkins, H, Lucassen, A, O'Kelly, I, Salmon, A, Bu'lock, F, Granados-Riveron, J, Setchfield, K, Thornborough, C, Brook, J, Mulder, B, Klaassen, S, Bhattacharya, S, Devriendt, K, Fitzpatrick, D, Wilson, D, Mital, S, Hurles, M