Associated Papers
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients.
Chesneau B et al.
Clinical Genetics, 2022
Peters plus syndrome mutations affect the function and stability of human β1,3-glucosyltransferase.
Zhang A et al.
The Journal of Biological Chemistry, 2021
Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome.
Weh E et al.
Plos One, 2017
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes.
Weh E et al.
Clinical Genetics, 2014
Two Tunisian patients with Peters plus syndrome harbouring a novel splice site mutation in the B3GALTL gene that modulates the mRNA secondary structure.
Siala O et al.
Gene, 2012
A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly.
Aliferis K et al.
Ophthalmic Genetics, 2010
Novel B3GALTL mutation in Peters-plus Syndrome.
Dassie-Ajdid J et al.
Clinical Genetics, 2009
Select a paper to view details