Molecular analysis of CYP1B1 in Omani patients with primary congenital glaucoma: a pilot study

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...

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Detalles Bibliográficos
Autores principales: El-Gayar, Stefan, Ganesh, Anuradha, Chavarria-Soley, Gabriela, Al-Zuhaibi, Sana, Al-Mjeni, Rayhanah, Raeburn, Sandy, Bialasiewicz, Alexander A.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709423/
https://www.ncbi.nlm.nih.gov/pubmed/19597567

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709423/
https://www.ncbi.nlm.nih.gov/pubmed/19597567

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