Associated Papers
FOXP4 Variants Are Associated With Plateau Iris and Angle Closure Glaucoma.
Presley W et al.
Investigative Ophthalmology & Visual Science, 2025
Inhibition of Foxp4 Disrupts Cadherin-based Adhesion of Radial Glial Cells, Leading to Abnormal Differentiation and Migration of Cortical Neurons in Mice.
Li X et al.
Neuroscience Bulletin, 2023
Recurrent FOXP4 nonsense variant in two unrelated patients: Association with neurodevelopmental disease and congenital diaphragmatic hernia.
Del Viso F et al.
American Journal of Medical Genetics. Part A, 2023
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities.
Snijders Blok L et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
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