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KCNQ2 Is a Nodal K(+) Channel
Mutations in the gene encoding the K(+) channel KCNQ2 cause neonatal epilepsy and myokymia, indicating that KCNQ2 regulates the excitability of CNS neurons and motor axons, respectively. We show here that KCNQ2 channels are functional components of axon initial segments and nodes of Ranvier, colocal...
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| Publicado no: | J Neurosci |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Society for Neuroscience
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6793582/ https://ncbi.nlm.nih.gov/pubmed/14762142 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4512-03.2004 |
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