Further Evidence for a Possible Role for ZFHX4 in Human Ocular Development and Disease
Am J Med Genet A
.
2025 Mar;197(3):e63911.
doi: 10.1002/ajmg.a.63911.
Epub 2024 Oct 25.
Authors
Linda M Reis
1
,
Gerald W Zaidman
2
,
Samuel Thompson
1
,
Sanaa Muheisen
1
,
Tom Glaser
3
,
Elena V Semina
1
4
5
Affiliations
1
Department of Ophthalmology and Visual Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
2
Department of Ophthalmology, New York Medical College, Westchester Medical Center, Valhalla, New York, USA.
3
Department of Cell Biology and Human Anatomy, University of California, Davis, California, USA.
4
Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Wisconsin, Milwaukee, Wisconsin, USA.
5
Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
PMID:
39450701
PMCID:
PMC11821440
(available on
2026-03-01
)
DOI:
10.1002/ajmg.a.63911
No abstract available
Keywords:
ZFHX4; 8q21.11 deletion; Peters anomaly; congenital corneal opacity.
Publication types
Letter
Grants and funding
R01 EY015518/EY/NEI NIH HHS/United States
R01 EY015518/NH/NIH HHS/United States
R01 EY034398/NH/NIH HHS/United States
RO1 EY033742/NH/NIH HHS/United States
R01 EY033742/EY/NEI NIH HHS/United States
R01 EY034398/EY/NEI NIH HHS/United States