Associated Papers
U2AF2 Missense Variant Associated With Epilepsy and Systemic Dysmorphism: Report of Two Cases and Literature Review.
Huang S et al.
Clinical Case Reports, 2025
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features.
Li D et al.
The Journal of Clinical Investigation, 2024
A de novo U2AF2 heterozygous variant associated with hypomyelinating leukodystrophy.
Kuroda Y et al.
American Journal of Medical Genetics. Part A, 2023
U2AF2 variant in a patient with developmental delay, dysmorphic features, and epilepsy.
Kittock CM et al.
American Journal of Medical Genetics. Part A, 2023
A presumed missense variant in the U2AF2 gene causes exon skipping in neurodevelopmental diseases.
Wang X et al.
Journal of Human Genetics, 2023
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM10_ESM.xlsx › Supplementary_Data_8
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