A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration
- Author(s):
- 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.
- Published
- 2013
- Publication type
- Article / Letter to editor
- Date issued
- 2013-11-30
- Language
- English
- Is part of
- Nature Genetics (2013), Vol. 45, no. 11, p. 1371-U153
- hdl
- 1887/102464
- doi
- 10.1038/ng.2740