Associated Papers
Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.
Wentling M et al.
Advanced Science (weinheim, Baden-wurttemberg, Germany), 2026
Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss.
Mendia C et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy, 2024
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans.
Vona B et al.
Human Genetics, 2021
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.
Dunbar LA et al.
Embo Molecular Medicine, 2019
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