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In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission
Benign familial neonatal epilepsy is a neuronal channelopathy most commonly caused by mutations in KCNQ2, which encodes the K(v)7.2 subunit of the slow K(+) channel. K(v)7.2 is expressed in both central and peripheral nervous systems. Seizures occur in the neonatal period, often in clusters within t...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3470715/ https://ncbi.nlm.nih.gov/pubmed/23065794 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/aws241 |
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