Article

SLC4A11 Revisited: Isoforms, Expression, Functions and Unresolved Questions

2025-05-13

Abstract excerpt

The SLC4A11 gene encodes a membrane transporter implicated in congenital hereditary endothelial dystrophy, Harboyan syndrome, and certain cancers. Despite its clinical importance, current data on SLC4A11 expression patterns, transcript variants, and functional roles remain inconsistent and sometimes contradictory. We have systematized existing data, identified areas of consensus, and highlighted discrepancies. Thi...

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Literature Corpus work: 9a2018eb-f658-594f-b6ed-0bc142013cea
DOI: 10.20944/preprints202505.1026.v1

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