Cargando…
Comprehensive characterization of DNA methylation changes in Fuchs endothelial corneal dystrophy
Transparency of the human cornea is necessary for vision. Fuchs Endothelial Corneal Dystrophy (FECD) is a bilateral, heritable degeneration of the corneal endothelium, and a leading indication for corneal transplantation in developed countries. While the early onset, and rarer, form of FECD has been...
Autores principales: | Khuc, Emily, Bainer, Russell, Wolf, Marie, Clay, Selene M., Weisenberger, Daniel J., Kemmer, Jacquelyn, Weaver, Valerie M., Hwang, David G., Chan, Matilda F. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383226/ https://www.ncbi.nlm.nih.gov/pubmed/28384203 http://dx.doi.org/10.1371/journal.pone.0175112 |
Ejemplares similares
-
Aberrant DNA methylation of miRNAs in Fuchs endothelial corneal dystrophy
por: Pan, Peipei, et al.
Publicado: (2019) -
Author Correction: Aberrant DNA methylation of miRNAs in Fuchs endothelial corneal dystrophy
por: Pan, Peipei, et al.
Publicado: (2020) -
Corneal Hydration Control in Fuchs' Endothelial Corneal Dystrophy
por: Wacker, Katrin, et al.
Publicado: (2016) -
The Genetic Basis of Fuchs Endothelial Corneal Dystrophy
por: Feizi, Sepehr
Publicado: (2010) -
Fuchs endothelial corneal dystrophy: current perspectives
por: Vedana, Gustavo, et al.
Publicado: (2016)