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A connexin30 mutation rescues hearing and reveals roles for gap junctions in cochlear amplification and micromechanics
Accelerated age-related hearing loss disrupts high-frequency hearing in inbred CD-1 mice. The p.Ala88Val (A88V) mutation in the gene coding for the gap-junction protein connexin30 (Cx30) protects the cochlear basal turn of adult CD-1Cx30(A88V/A88V) mice from degeneration and rescues hearing. Here we...
Autores principales: | Lukashkina, Victoria A., Levic, Snezana, Lukashkin, Andrei N., Strenzke, Nicola, Russell, Ian J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321796/ https://www.ncbi.nlm.nih.gov/pubmed/28220769 http://dx.doi.org/10.1038/ncomms14530 |
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