Myocilin Mutations Are Not a Major Cause of Primary Congenital Glaucoma in Iranian Patients

PURPOSE: To assess the frequency of mutations in the Myocilin (MYOC) gene in Iranian patients affected with primary congenital glaucoma (PCG). METHODS: The individuals evaluated herein are among a larger cohort of 100 patients who had previously been screened for CYP1B1 mutations. Eighty subjects ca...

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Detalles Bibliográficos
Autores principales: Elahi, Elahe, Narooie-Nejhad, Mehrnaz, Suri, Fatemeh, yazdani, Shahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ophthalmic Research Center 2010
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380681/
https://www.ncbi.nlm.nih.gov/pubmed/22737338

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380681/
https://www.ncbi.nlm.nih.gov/pubmed/22737338

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