Selection of Diagnostically Significant Regions of the <i>SLC26A4</i> Gene Involved in Hearing Loss
Screening pathogenic variants in the <i>SLC26A4</i> gene is an important part of molecular genetic testing for hearing loss (HL) since they are one of the common causes of hereditary HL in many populations. However, a large size of the <i>SLC26A4</i> gene (20 coding exons) pr...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-11-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/23/21/13453 |