Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss

Original language	English
Article number	13453
Journal	International Journal of Molecular Sciences
Volume	23
Issue number	21
DOIs	https://doi.org/10.3390/ijms232113453
Publication status	Published - Nov 2022

bioinformatic analysis, hearing loss, molecular testing, pathogenic variants, pendrin, SLC26A4, Humans, Mutation, Hearing Loss/diagnosis, Sulfate Transporters/genetics, Hearing Loss, Sensorineural/genetics, Deafness/genetics

ID: 39331363