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Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing

Maureen Wentling et al.
HAL (France) · Papers · License: Open Access
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Mechanoelectrical transduction, Clarin-1 and Clarin-2, Synaptopathy, Hearing phenotypic variability, 0, Usher syndrome type III, Ion homeostasis
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Record · ID 268702
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