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Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs’ endothelial corneal dystrophy

INTRODUCTION: The pathogenic role of variants in TCF4 and COL8A2 in causing Fuchs’ endothelial corneal dystrophy (FECD) is not controversial and has been confirmed by numerous studies. The causal role of other genes, SLC4A11, ZEB1, LOXHD1, and AGBL1, which have been reported to be associated with FE...

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Detalles Bibliográficos
Autores principales: Tsedilina, Tatiana Romanovna, Sharova, Elena, Iakovets, Valeriia, Skorodumova, Liubov Olegovna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333596/
https://www.ncbi.nlm.nih.gov/pubmed/37441688
http://dx.doi.org/10.3389/fmed.2023.1153122