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

IntroductionThe 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 FECD...

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Detalhes bibliográficos

Principais autores:	Tatiana Romanovna Tsedilina, Elena Sharova, Valeriia Iakovets, Liubov Olegovna Skorodumova
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Frontiers Media S.A. 2023-06-01
coleção:	Frontiers in Medicine
Assuntos:	Fuchs dystrophy SLC4A11 ZEB1 LOXHD1 AGBL1 posterior polymorphous corneal dystrophy type 3
Acesso em linha:	https://www.frontiersin.org/articles/10.3389/fmed.2023.1153122/full
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