Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness

Central corneal thickness (CCT), one of the most highly heritable human traits (h(2) typically>0.9), is important for the diagnosis of glaucoma and a potential risk factor for glaucoma susceptibility. We conducted genome-wide association studies in five cohorts from Australia and the United Kingd...

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Detalles Bibliográficos
Autores principales: Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J., Macgregor, Stuart, Craig, Jamie E., Mackey, David A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869325/
https://www.ncbi.nlm.nih.gov/pubmed/20485516
http://dx.doi.org/10.1371/journal.pgen.1000947

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869325/
https://www.ncbi.nlm.nih.gov/pubmed/20485516
http://dx.doi.org/10.1371/journal.pgen.1000947

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