A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction
Author:
Publisher
Elsevier BV
Subject
Sensory Systems
Reference29 articles.
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3. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1;Browne;Nature Genetics,1994
4. Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti;Carlisle;Gene Expression Patterns,2012
5. Vestibular hair cells and afferents: two channels for head motion signals;Eatock;Annual Review of Neuroscience,2011
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