MYOC and FOXC1 gene analysis in primary congenital glaucoma

PURPOSE: To screen the myocilin (MYOC) and forkhead box protein C1 (FOXC1) genes for sequence variations in primary congenital glaucoma (PCG). METHODS: Seventy five PCG patients were screened for MYOC variations and 54 cases (negative or heterozygous for cytochrome P4501B1 mutations) for FOXC1 mutat...

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Detalles Bibliográficos
Autores principales: Tanwar, Mukesh, Kumar, Manoj, Dada, Tanuj, Sihota, Ramanjit, Dada, Rima
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956699/
https://www.ncbi.nlm.nih.gov/pubmed/21031026

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956699/
https://www.ncbi.nlm.nih.gov/pubmed/21031026

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