Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol

PURPOSE: The gene coding cytochrome P4501B1 (CYP1B1) has been shown to be a major cause of primary congenital glaucoma in the Iranian population. More recently it was shown to also be important in juvenile-onset open angle glaucoma (JOAG). We aimed to further investigate the role of CYP1B1 in a larg...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Suri, Fatemeh, Kalhor, Reza, Zargar, Seyed Jalal, Nilforooshan, Navid, Yazdani, Shahin, Nezari, Hossein, Paylakhi, Seyed Hassan, Narooie-Nejhad, Mehrnaz, Bayat, Behnaz, Sedaghati, Tina, Ahmadian, Afshin, Elahi, Elahe
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Molecular Vision 2008
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2603445/
https://ncbi.nlm.nih.gov/pubmed/19096718
Tagiau: Ychwanegu Tag
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