Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder
- Author(s):
- Baca, M.D.P.; Palomares-Bralo, M.; Vanhooydonck, M.; Hamerlinck, L.; D'haene, E.; Leimbacher, S.; Jacobs, E.Z.; Cock, L. de; D'haenens, E.; Dheedene, A.; Malfait, Z.; Vantomme, L.; Silva, A.; Rooney, K.; Zhao, X.A.; Saeidian, A.H.; Owen, N.M.; Santos-Simarro, F.; Lleuger-Pujol, R.; Garcia-Minaur, S.; Losantos-Garcia, I.; Menten, B.; Gestri, G.; Ragge, N.; Consortium, Z.; Sadikovic, B.; Bogaert, E.; Vleminckx, K.; Naert, T.; Syx, D.; Callewaert, B.; Vergult, S.
- Published
- 2025
- Publication type
- Article / Letter to editor
- Date issued
- 2025-06-05
- Language
- English
- Publisher
- Elsevier
- Is part of
- American Journal of Human Genetics (2025), Vol. 112, no. 6, p. 1388-1414
- hdl
- 1887/4295802
- doi
- 10.1016/j.ajhg.2025.04.008
