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

Autor: 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.
Rok vydání: 2021
DOI: 10.6084/m9.figshare.14853011.v1
Popis: 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.
Databáze: OpenAIRE