Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction

Vertigo due to vestibular dysfunction is rare in children. The elucidation of its etiology will improve clinical management and the quality of life of patients. Genes for vestibular dysfunction were previously identified in patients with both hearing loss and vertigo. This study aimed to identify ra...

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Detalles Bibliográficos
Autores principales: Sumalde, Angelo Augusto M., Scholes, Melissa A., Kalmanson, Olivia A., Terhune, Elizabeth A., Frejo, Lidia, Wethey, Cambria I., Roman-Naranjo, Pablo, Carry, Patrick M., Gubbels, Samuel P., Lopez-Escamez, Jose A., Hadley-Miller, Nancy, Santos-Cortez, Regie Lyn P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137884/
https://www.ncbi.nlm.nih.gov/pubmed/37107589
http://dx.doi.org/10.3390/genes14040831

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137884/
https://www.ncbi.nlm.nih.gov/pubmed/37107589
http://dx.doi.org/10.3390/genes14040831

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