KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference44 articles.
1. How well do we understand the cochlea?
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4. Genes involved in deafness
5. KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness
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1. The potassium channel subunit KV1.8 (Kcna10) is essential for the distinctive outwardly rectifying conductances of type I and II vestibular hair cells;2024-09-04
2. The potassium channel subunit KV1.8 (Kcna10) is essential for the distinctive outwardly rectifying conductances of type I and II vestibular hair cells;2024-09-04
3. Vestibular hair cells are more prone to damage by excessive acceleration insult in the mouse with KCNQ4 dysfunction;Scientific Reports;2024-07-03
4. Cholinergic modulation in the vertebrate auditory pathway;Frontiers in Cellular Neuroscience;2024-06-19
5. Vestibular afferent neurons develop normally in the absence of quantal/glutamatergic input;2024-06-13
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