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

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: 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
Μορφή: Artigo
Γλώσσα:Αγγλικά
Έκδοση: 2013
Διαθέσιμο Online:https://doi.org/10.1038/ng.2758
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