Nervous system K(V)7 disorders: breakdown of a subthreshold brake

Voltage-gated K(+) channels of the K(V)7 (KCNQ) family have been identified in the last 10–15 years by discovering the causative genes for three autosomal dominant diseases: cardiac arrhythmia (long QT syndrome) with or without congenital deafness (KCNQ1), a neonatal epilepsy (KCNQ2 and KCNQ3) and p...

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Detalhes bibliográficos
Main Authors: Maljevic, Snezana, Wuttke, Thomas V, Lerche, Holger
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2008
Assuntos:
Symposium Section Reports: Kv7 (KCNQ) Potassium Channels that are Mutated in Human Diseases
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2375730/
https://ncbi.nlm.nih.gov/pubmed/18238816
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2008.150656
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