<i>SLC4A11</i> Revisited: Isoforms, Expression, Functions, and Unresolved Questions

<i>SLC4A11</i> Revisited: Isoforms, Expression, Functions, and Unresolved Questions

The <i>SLC4A11</i> gene encodes a membrane transporter implicated in congenital hereditary endothelial dystrophy, Harboyan syndrome, and certain cancers. Despite its clinical importance, current data on <i>SLC4A11</i> expression patterns, transcript variants, and functional r...

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Bibliographic Details
Main Authors: Polina Alekseevna Kovaleva, Elena Sergeevna Kotova, Elena Ivanovna Sharova, Liubov Olegovna Skorodumova
Format: Article
Language:English
Published: MDPI AG 2025-06-01
Series:Biomolecules
Subjects:
SLC4A11
congenital hereditary endothelial dystrophy
Harboyan syndrome
cornea
corneal endothelium
Fuchs endothelial corneal dystrophy
Online Access:https://www.mdpi.com/2218-273X/15/6/875
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