Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration(†)

Although numerous common age-related macular degeneration (AMD) alleles have been discovered using genome-wide association studies, substantial disease heritability remains unexplained. We sought to identify additional common and rare variants associated with advanced AMD. A total of 4,332 cases and...

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Опубликовано в: :Hum Mol Genet
Главные авторы: Yu, Yi, Wagner, Erin K., Souied, Eric H., Seitsonen, Sanna, Immonen, Ilkka J., Häppölä, Paavo, Raychaudhuri, Soumya, Daly, Mark J., Seddon, Johanna M.
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2016
Предметы:
Association Studies Articles
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6078639/
https://ncbi.nlm.nih.gov/pubmed/28011711
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw336
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