Copy Number Variation at Chromosome 5q21.2 Is Associated With Intraocular Pressure

PURPOSE. Glaucoma is a major cause of blindness in the world. Recent genome-wide association studies (GWAS) have identified common genetic variants for glaucoma, but still a significant heritability gap remains. We hypothesized that copy number variants (CNVs) might influence part of the susceptibil...

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Detalhes bibliográficos
Main Authors: Nag, Abhishek, Venturini, Cristina, Hysi, Pirro G., Arno, Matthew, Aldecoa-Otalora Astarloa, Estibaliz, MacGregor, Stuart, Hewitt, Alex W., Young, Terri L., Mitchell, Paul, Viswanathan, Ananth C., Mackey, David A., Hammond, Christopher J.
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4141707/
https://ncbi.nlm.nih.gov/pubmed/23599335
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.13-11952
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