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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...

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Detalles Bibliográficos
Autores principales:	Danilchenko, Valeriia Yu., Zytsar, Marina V., Maslova, Ekaterina A., Posukh, Olga L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
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

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