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Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss
Screening pathogenic variants in the SLC26A4 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 SLC26A4 gene (20 coding exons) predetermines the difficulties of its co...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655724/ https://www.ncbi.nlm.nih.gov/pubmed/36362242 http://dx.doi.org/10.3390/ijms232113453 |