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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Detalles Bibliográficos
Autores principales: Liu, Xuerui, Zheng, Tao, Zhao, Chuchu, Zhang, Yi, Liu, Hanruo, Wang, Liyuan, Liu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204469/
https://www.ncbi.nlm.nih.gov/pubmed/34130750
http://dx.doi.org/10.1186/s40662-021-00246-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204469/
https://www.ncbi.nlm.nih.gov/pubmed/34130750
http://dx.doi.org/10.1186/s40662-021-00246-2

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