Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: Three novel mutations in CYP1B1

PURPOSE: To investigate the contribution of cytochrome P4501B1 (CYP1B1) and myocillin (MYOC) mutations to primary congenital glaucoma (PCG) in Moroccan families. METHODS: This study included 90 unrelated families with PCG and 100 normal control individuals. Two previously reported CYP1B1 mutations (...

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Autors principals: Hilal, Latifa, Boutayeb, Soraya, Serrou, Aziza, Refass-Buret, Loubna, Shisseh, Hafsa, Bencherifa, Fatiha, El Mzibri, Mohammed, Benazzouz, Bouchra, Berraho, Amina
Format: Artigo
Idioma:Inglês
Publicat: Molecular Vision 2010
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Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2901188/
https://ncbi.nlm.nih.gov/pubmed/20664688
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