Genetic and functional involvement of ZEB1 and FEN1 genes in FECD pathogenesis
Fuchs’ endothelial corneal dystrophy (FECD) is a dominantly inherited complex disorder, clinically manifested as thickened collagenous deposition on corneal Descemet’s membrane with excrescences called guttae [1, 2]. The current study intends to understand the genetic and functional role of FECD can...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Science Planet Inc.
2017-10-01
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| Series: | Canadian Journal of Biotechnology |
| Online Access: | https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue/cjb.2017-a95.pdf |