Associated Papers
In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene.
Vetriselvan Y et al.
Biochemical Genetics, 2025
Deletion of exon 4 of the PITX2 in a child with Axenfeld-Rieger syndrome.
Tian Y et al.
Ophthalmic Genetics, 2024
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations.
D'haene B et al.
Investigative Ophthalmology & Visual Science, 2011
Select a paper to view details