Screening of CYP1B1 Arg368His as predominant mutation in North Indian primary open angle glaucoma and juvenile onset glaucoma patients

In India, mutations in Cytochrome P450 (CYP1B1) are a predominant cause of not only primary congenital glaucoma (PCG) but also involved in primary open angle glaucoma (POAG) and juvenile onset glaucoma (JOAG). After ethical clearance, 100 POAG patients, 30 primary angle closure glaucoma (PACG) patie...

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Detalles Bibliográficos
Autores principales: Kaur, Avneet, Vanita, Vanita, Singh, JaiRup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363938/
https://www.ncbi.nlm.nih.gov/pubmed/30788381
http://dx.doi.org/10.22099/mbrc.2018.30630.1344

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363938/
https://www.ncbi.nlm.nih.gov/pubmed/30788381
http://dx.doi.org/10.22099/mbrc.2018.30630.1344

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