Exome-based investigation of the genetic basis of human pigmentary glaucoma

Exome-based investigation of the genetic basis of human pigmentary glaucoma

Abstract Background Glaucoma is a leading cause of visual disability and blindness. Release of iris pigment within the eye, pigment dispersion syndrome (PDS), can lead to one type of glaucoma known as pigmentary glaucoma. PDS has a genetic component, however, the genes involved with this condition a...

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Main Authors: 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
Format: Article
Language:English
Published: BMC 2021-06-01
Series:BMC Genomics
Subjects:
Pigmentary Glaucoma
Pigment dispersion syndrome
Glaucoma
Exomes
Human genetics
Online Access:https://doi.org/10.1186/s12864-021-07782-0

Internet

https://doi.org/10.1186/s12864-021-07782-0

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