Cargando…
Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy
The aim of the present study was to determine the genetic basis of a multi-generational family with late-onset (LO) Fuchs corneal dystrophy (FCD). Five FCD causal genes [solute carrier family 4, sodium borate transporter, member 11 (SLC4A11), zinc finger E-box binding homeobox 1 (ZEB1), lipoxygenase...
Autores principales: | TANG, HUI, ZHANG, WEN, YAN, XIN-MIN, WANG, LIN-PING, DONG, HONG, SHOU, TAO, LEI, HUO, GUO, QIANG |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866966/ https://www.ncbi.nlm.nih.gov/pubmed/27121161 http://dx.doi.org/10.3892/ijmm.2016.2570 |
Ejemplares similares
-
Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs’ endothelial corneal dystrophy
por: Tsedilina, Tatiana Romanovna, et al.
Publicado: (2023) -
Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India
por: Gupta, Ranjan, et al.
Publicado: (2015) -
Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy
por: Igo, Robert P., et al.
Publicado: (2012) -
Replication of TCF4 through Association and Linkage
Studies in Late-Onset Fuchs Endothelial Corneal Dystrophy
por: Li, Yi-Ju, et al.
Publicado: (2011) -
CTG18.1 Expansion in TCF4 Among African Americans With Fuchs' Corneal Dystrophy
por: Eghrari, Allen O., et al.
Publicado: (2017)