Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction

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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Bibliographic Details
Main Authors: Angelo Augusto M. Sumalde, Melissa A. Scholes, Olivia A. Kalmanson, Elizabeth A. Terhune, Lidia Frejo, Cambria I. Wethey, Pablo Roman-Naranjo, Patrick M. Carry, Samuel P. Gubbels, Jose A. Lopez-Escamez, Nancy Hadley-Miller, Regie Lyn P. Santos-Cortez
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Genes
Subjects:
balance disorder
dizziness
<i>HMX3</i>
<i>LAMA2</i>
Meniere’s disease
<i>OTOP1</i>
Online Access:https://www.mdpi.com/2073-4425/14/4/831

Internet

https://www.mdpi.com/2073-4425/14/4/831

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