Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma

Abstract

Mutations in the CYP1B1 gene are currently the main known genetic cause of primary congenital glaucoma (PCG), a leading cause of blindness in children. Here, we analyze for the first time the CYP1B1 genotype activity and the microscopic and clinical phenotypes in human PCG. Surgical pieces from trabeculectomy from patients with PCG (n = 5) and sclerocorneal… (More)
DOI: 10.1371/journal.pone.0176386

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