CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma

Introduction: Primary open-angle glaucoma (POAG) is a leading cause of visual impairment worldwide and a complex genetic disorder that affects mostly adults. Mutations in the MYOCILIN (MYOC) and OPTINEURIN genes account for rare forms with a Mendelian inheritance and for <5% of all POAG cases. Th...

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Main Authors: Melki, R, Colomb, E, Lefort, N, Brezin, A, Garchon, H
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Group 2004
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Original Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735887/
https://ncbi.nlm.nih.gov/pubmed/15342693
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.020024
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