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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Huvudupphovsmän: Lee, Sue I., Conrad, Travis, Jones, Sherri M., Lagziel, Ayala, Starost, Matthew F., Belyantseva, Inna A., Friedman, Thomas B., Morell, Robert J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2013
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Article
Länkar: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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