Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies

Pathogenic variants in the SLC26A4, FOXI1, and KCNJ10 genes are associated with hearing loss (HL) and specific inner ear abnormalities (DFNB4). In the present study, phenotype analyses, including clinical data collection, computed tomography (CT), and audiometric examination, were performed on deaf...

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Detalles Bibliográficos
Autores principales: Klarov, Leonid A., Pshennikova, Vera G., Romanov, Georgii P., Cherdonova, Aleksandra M., Solovyev, Aisen V., Teryutin, Fedor M., Luginov, Nikolay V., Kotlyarov, Petr M., Barashkov, Nikolay A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740095/
https://www.ncbi.nlm.nih.gov/pubmed/36499699
http://dx.doi.org/10.3390/ijms232315372

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740095/
https://www.ncbi.nlm.nih.gov/pubmed/36499699
http://dx.doi.org/10.3390/ijms232315372

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