Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay

Research output: Contribution to journal › Article › peer-review

Original language	English
Article number	10732
Number of pages	16
Journal	International Journal of Molecular Sciences
Volume	26
Issue number	21
DOIs	https://doi.org/10.3390/ijms262110732
Publication status	Published - 4 Nov 2025

Humans, Sulfate Transporters/genetics, Male, Female, Mutation, Hearing Loss, Sensorineural/genetics, Hearing Loss/genetics, RNA Splicing, Exons, Siberia, Goiter, Nodular

ID: 72240044