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Genetic mutations and molecular mechanisms of Fuchs endothelial corneal dystrophy
BACKGROUND: Fuchs endothelial corneal dystrophy is a hereditary disease and the most frequent cause of corneal transplantation in the worldwide. Its main clinical signs are an accelerated decrease in the number of endothelial cells, thickening of Descemet’s membrane and formation of guttae in the ex...
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| Publicat a: | Eye Vis (Lond) |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8204469/ https://ncbi.nlm.nih.gov/pubmed/34130750 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40662-021-00246-2 |
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