Associated Papers
De Novo SLC12A2 Variant Presenting as Congenital Hearing Loss With Vestibular Areflexia.
Ludin K et al.
American Journal of Medical Genetics. Part A, 2025
Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families.
Adadey SM et al.
Frontiers in Genetics, 2022
SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect.
McNeill A et al.
Brain : a Journal of Neurology, 2020
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