Associated Papers
Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the Israeli population.
Geyer O et al.
American Journal of Ophthalmology, 2011
Novel CYP1B1 and known PAX6 mutations in anterior segment dysgenesis (ASD).
Chavarria-Soley G et al.
Journal of Glaucoma, 2006
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients.
Sitorus R et al.
Journal of Medical Genetics, 2003
A novel truncating mutation of cytochrome P4501B1 (CYP1B1) gene in primary infantile glaucoma.
Kakiuchi T et al.
American Journal of Ophthalmology, 1999
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1.
Stoilov I et al.
American Journal of Human Genetics, 1998
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