M Channel KCNQ2 Subunits Are Localized to Key Sites for Control of Neuronal Network Oscillations and Synchronization in Mouse Brain

Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy. In heterologous cells, KCNQ2 expression yields voltage-gated potassium channels that activate slowly (τ, ∼0.1 sec) at subthreshold membrane potentials....

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Bibliografiska uppgifter
I publikationen:J Neurosci
Huvudupphovsmän: Cooper, Edward C., Harrington, Emily, Jan, Yuh Nung, Jan, Lily Y.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Society for Neuroscience 2001
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ARTICLE
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6763050/
https://ncbi.nlm.nih.gov/pubmed/11739564
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.21-24-09529.2001
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