Genomics

Dataset Information

0

Genetic variants associated with development of pseudoexfoliation syndrome


ABSTRACT: Pseudoexfoliation syndrome (PEXS) is a late-onset disorder in which fibrillar material accumulates at abnormally high concentrations mainly in the anterior segment of the eye. PEXS is the most common cause of secondary glaucoma, which can ultimately lead to blindness and is associated with a higher risk of cataract and serious complications following different types of intraocular surgery. Although PEXS clearly has a genetic component, it remains poorly explored. In our genome-wide association study, we searched for an association of genetic variants with this disorder among older Poles with PEXS without glaucoma.

ORGANISM(S): Homo sapiens

PROVIDER: GSE93205 | GEO | 2018/01/31

REPOSITORIES: GEO

Dataset's files

Source:
Action DRS
Other
Items per page:
1 - 1 of 1

Similar Datasets

2016-05-23 | PXD002623 | Pride
2017-03-31 | MSV000080838 | MassIVE
2020-10-27 | GSE135655 | GEO
2020-10-27 | GSE135653 | GEO
2020-10-27 | GSE135656 | GEO
2020-10-27 | GSE135654 | GEO
2014-01-17 | PXD000198 | Pride
2020-10-27 | GSE135658 | GEO
2023-12-18 | MSV000093682 | MassIVE
2016-01-04 | PXD000787 | Pride