Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.

Pérez Baca MDR, Palomares-Bralo M, Vanhooydonck M, Hamerlinck L, D'haene E, Leimbacher S, Jacobs EZ, De Cock L, D'haenens E, Dheedene A, Malfait Z, Vantomme L, Silva A, Rooney K, Zhao X, Saeidian AH, Owen NM, Santos-Simarro F, Lleuger-Pujol R, García-Miñaúr S, Losantos-García I, Menten B, Gestri G, Ragge N, ZFHX4 consortium, Sadikovic B, Bogaert E, Vleminckx K, Naert T, Syx D, Callewaert B, Vergult S

Open source

DOI: 10.1016/j.ajhg.2025.04.008
Published: 2025 Jun 5
Container: American journal of human genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1016/j.ajhg.2025.04.008,
  title = {Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.},
  author = {Pérez Baca MDR and Palomares-Bralo M and Vanhooydonck M and Hamerlinck L and D'haene E and Leimbacher S and Jacobs EZ and De Cock L and D'haenens E and Dheedene A and Malfait Z and Vantomme L and Silva A and Rooney K and Zhao X and Saeidian AH and Owen NM and Santos-Simarro F and Lleuger-Pujol R and García-Miñaúr S and Losantos-García I and Menten B and Gestri G and Ragge N and ZFHX4 consortium and Sadikovic B and Bogaert E and Vleminckx K and Naert T and Syx D and Callewaert B and Vergult S},
  year = {2025},
  journal = {American journal of human genetics},
  doi = {10.1016/j.ajhg.2025.04.008},
  url = {https://doi.org/10.1016/j.ajhg.2025.04.008}
}

RIS

TY  - JOUR
TI  - Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.
AU  - Pérez Baca MDR
AU  - Palomares-Bralo M
AU  - Vanhooydonck M
AU  - Hamerlinck L
AU  - D'haene E
AU  - Leimbacher S
AU  - Jacobs EZ
AU  - De Cock L
AU  - D'haenens E
AU  - Dheedene A
AU  - Malfait Z
AU  - Vantomme L
AU  - Silva A
AU  - Rooney K
AU  - Zhao X
AU  - Saeidian AH
AU  - Owen NM
AU  - Santos-Simarro F
AU  - Lleuger-Pujol R
AU  - García-Miñaúr S
AU  - Losantos-García I
AU  - Menten B
AU  - Gestri G
AU  - Ragge N
AU  - ZFHX4 consortium
AU  - Sadikovic B
AU  - Bogaert E
AU  - Vleminckx K
AU  - Naert T
AU  - Syx D
AU  - Callewaert B
AU  - Vergult S
PY  - 2025
JO  - American journal of human genetics
DO  - 10.1016/j.ajhg.2025.04.008
UR  - https://doi.org/10.1016/j.ajhg.2025.04.008
ER  -

APA

MDR, P. B., M, P., M, V., L, H., E, D., S, L., EZ, J., L, D. C., E, D., A, D., Z, M., L, V., A, S., K, R., X, Z., AH, S., NM, O., F, S., R, L., S, G., I, L., B, M., G, G., N, R., consortium, Z., B, S., E, B., K, V., T, N., D, S., B, C., & S, V. (2025). Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2025.04.008

Source records

pubmed · retrieved 2026-09-25T19:30:41.941Z
europe-pmc · retrieved 2026-09-25T19:30:41.958Z