Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma

PURPOSE: To elucidate the incidence of cytochrome P450 1B1 (CYP1B1) and myocillin (MYOC) mutations in Korean patients with primary congenital glaucoma (PCG). METHODS: Genomic DNA was collected from peripheral blood of 85 unrelated Korean patients who were diagnosed as having PCG by standard ophthalm...

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Detalles Bibliográficos
Autores principales: Kim, Hee-Jung, Suh, Wool, Park, Sung Chul, Kim, Chan Yun, Park, Ki Ho, Kook, Michael S., Kim, Yong Yeon, Kim, Chang-Sik, Park, Chan Kee, Ki, Chang-Seok, Kee, Changwon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156779/
https://www.ncbi.nlm.nih.gov/pubmed/21850185

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156779/
https://www.ncbi.nlm.nih.gov/pubmed/21850185

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