 | Up a level |
2013
Helgason, Hannes, Sulem, Patrick, Duvvari, Maheswara R., Luo, Hongrong, Thorleifsson, Gudmar, Stefansson, Hreinn 
ORCID: 0000-0002-9331-6666, Jonsdottir, Ingileif, Masson, Gisli, Gudbjartsson, Daniel F., Walters, G. Bragi ORCID: 0000-0002-5415-6487, Magnusson, Olafur Th, Kong, Augustine ORCID: 0000-0001-8193-5438, Rafnar, Thorunn, Kiemeney, Lambertus A. ORCID: 0000-0002-2368-1326, Schoenmaker-Koller, Frederieke E., Zhao, Ling, Boon, Camiel J. F., Song, Yaojun, Fauser, Sascha, Pei, Michelle, Ristau, Tina, Patel, Shirrina, Liakopoulos, Sandra, van de Ven, Johannes P. H., Hoyng, Carel B., Ferreyra, Henry, Duan, Yaou, Bernstein, Paul S., Geirsdottir, Asbjorg, Helgadottir, Gudleif, Stefansson, Einar, den Hollander, Anneke I., Zhang, Kang ORCID: 0000-0002-4549-1697, Jonasson, Fridbert, Sigurdsson, Haraldur, Thorsteinsdottir, Unnur and Stefansson, Kari
(2013).
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.
Nature Genet., 45 (11).
S. 1371 - 1377.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 1546-1718