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Compound heterozygous mutations in CYP1B1 gene leads to severe primary congenital glaucoma phenotype

12 Jun 2019

Abstract excerpt

AIM: To identify the novel mutation alleles in the CYP1B1 gene of primary congenital glaucoma (PCG) patients at Shandong Province of China, and investigate their correlation with glaucomatous features. METHODS: The DNA from the peripheral blood of 13 congenital glaucoma patients and 50 ethnically matched healthy controls from the affiliated hospital of Qingdao University were extracted. The coding region of the...

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PMID: 31236345
DOI: 10.18240/ijo.2019.06.05

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