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Article

Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma.

Molecular vision - 1 Jan 2009

Yang Mei, Guo Xiangming, Liu Xing, Shen Huangxuan, Jia Xiaoyun, Xiao Xueshan, Li Shiqiang, Fang Shaohua, Zhang Qingjiong

Abstract excerpt

PURPOSE: This study was conducted to investigate the mutation spectrum of the cytochrome P450 gene (CYP1B1) in Chinese patients with primary congenital glaucoma (PCG). METHODS: The coding regions of CYP1B1 from 41 Chinese PCG patients were analyzed using polymerase chain reaction (PCR) and heteroduplex analysis-single strand conformation polymorphism (HA-SSCP) followed by subsequent cloning and bidirectional...

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Identifiers

PMID: 19247456
PMCID: PMC2647971

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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