Energy Shortage in Human and Mouse Models of SLC4A11-Associated Corneal Endothelial Dystrophies

PURPOSE: To elucidate the molecular events in solute carrier family 4 member 11 (SLC4A11)-deficient corneal endothelium that lead to the endothelial dysfunction that characterizes the dystrophies associated with SLC4A11 mutations, congenital hereditary endothelial dystrophy (CHED) and Fuchs endothel...

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Detalhes bibliográficos
Publicado no:Invest Ophthalmol Vis Sci
Main Authors: Zhang, Wenlin, Frausto, Ricardo, Chung, Doug D., Griffis, Christopher G., Kao, Liyo, Chen, Angela, Azimov, Rustam, Sampath, Alapakkam P., Kurtz, Ira, Aldave, Anthony J.
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2020
Assuntos:
Cornea
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7425690/
https://ncbi.nlm.nih.gov/pubmed/32721020
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.61.8.39
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