Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

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Main Authors: Xiaowei Zhan, David E. Larson, Chaolong Wang, Daniel C. Koboldt, Yuri V. Sergeev, Robert S. Fulton, Lucinda Fulton, Catrina C. Fronick, Kari Branham, Jennifer L. Bragg‐Gresham, Goo Jun, Youna Hu, Hyun Min Kang, Dajiang J. Liu, Mohammad Othman, Matthew Brooks, Rinki Ratnapriya, Alexis Boleda, Felix Graßmann, Claudia von Strachwitz, Lana M. Olson, Gabriëlle H.S. Buitendijk, Albert Hofman, Cornelia M. van Duijn, Valentina Cipriani, Anthony T. Moore, Humma Shahid, Yingda Jiang, Yvette P. Conley, Denise J. Morgan, Ivana K. Kim, Matthew P. Johnson, Stuart Cantsilieris, Andrea J. Richardson, Robyn H. Guymer, Hongrong Luo, Hong Ouyang, Christoph Licht, Fred G. Pluthero, Mindy M Zhang, Kang Zhang, Paul N. Baird, John Blangero, Michael L. Klein, Lindsay A. Farrer, Margaret M. DeAngelis, Daniel E. Weeks, Michael B. Gorin, John R.W. Yates, Caroline C. W. Klaver, Margaret A. Pericak‐Vance, Jonathan L. Haines, Bernhard H. F. Weber, Richard K. Wilson, John R. Heckenlively, Emily Y. Chew, Dwight Stambolian, Elaine R. Mardis, Anand Swaroop, Gonçalo R. Abecasis
格式: Artigo
語言:英语
出版: 2013
在線閱讀:https://doi.org/10.1038/ng.2758
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