Identification of a Novel Isoform of Slc26a4 by Single-Cell RNA-sequencing of Pendrin-Expressing Cells in the Cochlea

Pathogenic variation of SLC26A4 gene causes both Pendred syndrome (PDS) and non-syndromic enlarged vestibular aqueduct (NSEVA/DFNB4), two autosomal recessive disorders. The former accounts for approximately 6