Exome-based investigation of the genetic basis of human pigmentary glaucoma
Exome-based investigation of the genetic basis of human pigmentary glaucoma
About this item
Full title
Author / Creator
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 and Fingert, John H
Publisher
London: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
London: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
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 are largely unknown. We sought to discover genes that cause PDS by test...
Alternative Titles
Full title
Exome-based investigation of the genetic basis of human pigmentary glaucoma
Authors, Artists and Contributors
Author / Creator
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
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_ce7f241b20c8405bb3d1d6a9635ffb16
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ce7f241b20c8405bb3d1d6a9635ffb16
Other Identifiers
ISSN
1471-2164
E-ISSN
1471-2164
DOI
10.1186/s12864-021-07782-0
