Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patients

PURPOSE: Mutations in Cytochrome P450 (CYP1B1) are a predominant cause of congenital glaucoma. This study was planned with the aim to identify the mutation profile of CYP1B1 in North Indian primary congenital glaucoma (PCG) patients. METHODS: After ethical clearance, 50 congenital glaucoma patients...

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Detalles Bibliográficos
Autores principales: Tanwar, Mukesh, Dada, Tanuj, Sihota, Ramanjit, Das, Taposh K., Yadav, Usha, Dada, Rima
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697458/
https://www.ncbi.nlm.nih.gov/pubmed/19536304

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697458/
https://www.ncbi.nlm.nih.gov/pubmed/19536304

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