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A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction
KCNA10 is a voltage gated potassium channel that is expressed in the inner ear. The localization and function of KCNA10 was studied in a mutant mouse, B6-Kcna10(TM45), in which the single protein coding exon of Kcna10 was replaced with a beta-galactosidase reporter cassette. Under the regulatory con...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3684051/ https://ncbi.nlm.nih.gov/pubmed/23528307 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.heares.2013.02.009 |
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