High expression of the underexplored SLC4A11 protein-coding transcript is specific to the corneal endothelium

Abstract Fuchs’ endothelial corneal dystrophy (FECD) and congenital hereditary endothelial dystrophy (CHED) are corneal endothelial pathologies associated with SLC4A11 gene variants. The principal findings on the expression and function of SLC4A11 in the corneal endothelium have been based on studie...

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Detalhes bibliográficos

Principais autores:	Elena S. Kotova, Elena I. Sharova, Polina A. Kovaleva, Boris E. Malyugin, Olga P. Antonova, Alexandra V. Belodedova, Ivan S. Tkachenko, Yuriy V. Doludin, Tatiana N. Garmanova, Mikhail Protasov, Tatiana R. Tsedilina, Liubov O. Skorodumova
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Nature Portfolio 2026-05-01
coleção:	Scientific Reports
Assuntos:	SLC4A11 Corneal endothelium Fuchs corneal dystrophy Transcription initiation Congenital hereditary endothelial dystrophy
Acesso em linha:	https://doi.org/10.1038/s41598-026-51987-w
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