Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma

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 heterodup...

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Detalles Bibliográficos
Autores principales: Yang, Mei, Guo, Xiangming, Liu, Xing, Shen, Huangxuan, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Fang, Shaohua, Zhang, Qingjiong
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647971/
https://www.ncbi.nlm.nih.gov/pubmed/19247456

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647971/
https://www.ncbi.nlm.nih.gov/pubmed/19247456

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