Article
Molecular analysis of CYP1B1 in Omani patients with primary congenital glaucoma: a pilot study.
Molecular vision - 8 Jul 2009
El-Gayar Stefan, Ganesh Anuradha, Chavarria-Soley Gabriela, Al-Zuhaibi Sana, Al-Mjeni Rayhanah, Raeburn Sandy, Bialasiewicz Alexander A
Abstract excerpt
PURPOSE: To screen cytochrome P4501B1 (CYP1B1) for causative mutations in Omani patients with a clinical diagnosis of primary congenital glaucoma (PCG) METHODS: Nine PCG families were recruited for the study. All patients underwent detailed clinical examinations to confirm the diagnosis of PCG. The families of index patients were also examined. Genealogical information was obtained by pedigree analysis. The...
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