Open access
Jul 2026
Identification of a novel isoform of Slc26a4 by single-cell RNA-sequencing of pendrin-expressing cells in the cochlea
It is demonstrated that the short Slc26a4 isoform is expressed in both the inner ear and kidney and investigated its interactions and functions, and the genotype-phenotype association for SLC26A4-related hearing loss is characterized in the context of these two isoforms.
J. Koh, C. Affortit, K. Homma et al.
· Human Genetics · 0 citations