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...

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Bibliographic Details
Main Authors: Valeriia Yu. Danilchenko, Marina V. Zytsar, Ekaterina A. Maslova, Olga L. Posukh
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