Further Evidence for a Possible Role for ZFHX4 in Human Ocular Development and Disease
- PMID: 39450701
- PMCID: PMC11821440
- DOI: 10.1002/ajmg.a.63911
Further Evidence for a Possible Role for ZFHX4 in Human Ocular Development and Disease
Keywords: ZFHX4; 8q21.11 deletion; Peters anomaly; congenital corneal opacity.
Conflict of interest statement
References
-
- Ben Ayed I, Bouzid A, Kammoun F, Souissi A, Jallouli O, Mallouli S, Guidara S, Loukil S, Aloulou H, Jbeli F et al. . 2021. 8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects. Mol Genet Genomic Med 9(11):e1811. 10.1002/mgg3.1811 - DOI - PMC - PubMed
-
- Creton M, Wagener F, Massink M, Fennis W, Bloemen M, Schols J, Aarts M, van der Molen AM, van Haaften G, van den Boogaard MJ. 2023. Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10. Am J Med Genet A 191(4):1083–1088. 10.1002/ajmg.a.63101 - DOI - PubMed
-
- Delea M, Massara LS, Espeche LD, Bidondo MP, Barbero P, Oliveri J, Brun P, Fabro M, Galain M, Fernandez CS et al. 2022. Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease. Genes (Basel) 13(7). 10.3390/genes13071172 - DOI - PMC - PubMed