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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...
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. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
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 |
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