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A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall
Digenic Connexin26 (Cx26, GJB2) and Cx30 (GJB6) heterozygous mutations are the second most frequent cause of recessive deafness in humans. However, the underlying deafness mechanism remains unclear. In this study, we created different double Cx26 and Cx30 heterozygous (Cx26(+/−)/Cx30(+/−)) mouse mod...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Neurobiol Dis |
|---|---|
| Prif Awduron: | , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2017
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5675824/ https://ncbi.nlm.nih.gov/pubmed/28823936 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2017.08.002 |
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