Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD

Authors

Erin K. Wagner, Tufts University
Soumya Raychaudhuri, University of Manchester
Mercedes B. Villalonga, Tufts University
Anuja Java, Washington University School of Medicine in St. Louis
Michael P. Triebwasser, Washington University School of Medicine in St. Louis
Mark J. Daly, Broad Institute
John P. Atkinson, Washington University School of Medicine in St. Louis
Johanna M. Seddon, Tufts University

Journal

Scientific Reports

Publication Date

2016

Volume

6

Inclusive Pages

31531

Document Type

Open Access Publication

DOI

10.1038/srep31531

Rights and Permissions

E.K. Wagner, et al. 30 August 2016. Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD. Scientific reports. Art. No. 31531. DOI: 10.1038/srep31531. http://www.nature.com/articles/srep31531

Recommended Citation

Wagner, Erin K.; Raychaudhuri, Soumya; Villalonga, Mercedes B.; Java, Anuja; Triebwasser, Michael P.; Daly, Mark J.; Atkinson, John P.; and Seddon, Johanna M., "Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD." Scientific Reports. 6, 31531. (2016).
https://digitalcommons.wustl.edu/open_access_pubs/5213