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A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration
- All authors
- Helgason, H.; Sulem, P.; Duvvari, M.R.; Luo, H.R.; Thorleifsson, G.; Stefansson, H.; Jonsdottir, I.; Masson, G.; Gudbjartsson, D.F.; Walters, G.B.; Magnusson, O.T.; Kong, A.; Rafnar, T.; Kiemeney, L.A.; Schoenmaker-Koller, F.E.; Zhao, L.; Boon, C.J.F.; Song, Y.J.; Fauser, S.; Pei, M.; Ristau, T.; Patel, S.; Liakopoulos, S.; Ven, J.P.H. van de; Hoyng, C.B.; Ferreyra, H.; Duan, Y.; Bernstein, P.S.; Geirsdottir, A.; Helgadottir, G.; Stefansson, E.; Hollander, A.I. den; Zhang, K.; Jonasson, F.; Sigurdsson, H.; Thorsteinsdottir, U.; Stefansson, K.
- Date
- 2013-11-30
- Journal
- Nature Genetics
- Volume
- 45
- Issue
- 11
- Pages
- 1371 - U153