Additional file 2 of Exome-based investigation of the genetic basis of human pigmentary glaucoma

van der Heide, Carly; Goar, Wes; Meyer, Kacie J.; Alward, Wallace L. M.; Boese, Erin A.; Sears, Nathan C.; Roos, Ben R.; Kwon, Young H.; DeLuca, Adam P.; Siggs, Owen M.; Gonzaga-Jauregui, Claudia; Sheffield, Val C.; Wang, Kai; Stone, Edwin M.; Mullins, Robert F.; Anderson, Michael G.; Fan, Bao Jian; Ritch, Robert; Craig, Jamie E.; Wiggs, Janey L.; Scheetz, Todd E.; Fingert, John H.

doi:10.6084/m9.figshare.14853011.v1

12864_2021_7782_MOESM2_ESM.docx (15.79 kB)

Additional file 2 of Exome-based investigation of the genetic basis of human pigmentary glaucoma

journal contribution

posted on 2021-06-27, 03:16 authored by Carly van der Heide, Wes Goar, Kacie J. Meyer, Wallace L. M. Alward, Erin A. Boese, Nathan C. Sears, Ben R. Roos, Young H. Kwon, Adam P. DeLuca, Owen M. Siggs, Claudia Gonzaga-Jauregui, Val C. Sheffield, Kai Wang, Edwin M. Stone, Robert F. Mullins, Michael G. Anderson, Bao Jian Fan, Robert Ritch, Jamie E. Craig, Janey L. Wiggs, Todd E. Scheetz, John H. Fingert

Additional file 2: Supplementary Table 2. Secondary analysis: mutations detected in candidate genes. Single instances of loss-of-function mutations were detected in three of the candidate genes in the secondary analysis.