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Hypothesis of K(+)-Recycling Defect Is Not a Primary Deafness Mechanism for Cx26 (GJB2) Deficiency
K(+)-recycling defect is a long-standing hypothesis for deafness mechanism of Connexin26 (Cx26, GJB2) mutations, which cause the most common hereditary deafness and are responsible for >50% of nonsyndromic hearing loss. The hypothesis states that Cx26 deficiency may disrupt inner ear gap junction...
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| Publicat a: | Front Mol Neurosci |
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| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5445178/ https://ncbi.nlm.nih.gov/pubmed/28603488 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2017.00162 |
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