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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Tanwar, Mukesh, Kumar, Manoj, Dada, Tanuj, Sihota, Ramanjit, Dada, Rima
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Molecular Vision 2010
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2956699/
https://ncbi.nlm.nih.gov/pubmed/21031026
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