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KCNQ3 gene

Known as: Kv7.3, POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 3, potassium voltage-gated channel subfamily Q member 3 
National Institutes of Health

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KCNQ3 Potassium Channel

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Retigabine-ezogabine: A new treatment option for bipolar disorder?
The M-channels (i.e., voltage-gated potassium channels formed by KCNQ2, KCNQ3 and KCNQ 5) has emerged as a promising target for… 
2015
2015
The Role of the Carboxyl Terminus Helix C-D Linker in Regulating KCNQ3 K+ Current Amplitudes by Controlling Channel Trafficking
In the central and peripheral nervous system, the assembly of KCNQ3 with KCNQ2 as mostly heteromers, but also homomers, underlies… 
2012
2012
Benign Neonatal Sleep Myoclonus
Benign neonatal sleep myoclonus is an uncommon, nonepileptic disorder characterized by myoclonic jerks appearing in the neonatal… 
2011
2011
Phenotype and Genotype Relationship between Inherited Cardiac Arrhythmia and Epileptic Syndrome
Inherited channel disorders are associated with paroxysmal dysfunction of excitable tissues and manifest as diseases of the heart… 
2009
2009
FP38-WE-02 Genetic study of juvenile myoclonic epilepsy (JME) patients and their family members in a university hospital in North India
2006
2006
Structural and functional correlation of the pore region of KCNQ3 channel in the brain neurons
2004
2004
Novel mutations in the KCNQ 2 gene link epilepsy to a dysfunction of the KCNQ 2-calmodulin interaction
M utations in the voltage gated potassium channels KCNQ2 (OMIM 602235) and KCNQ3 (OMIM 602232) are associated with an autosomal… 
2003
2003
Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population
Juvenile myoclonic epilepsy (JME) is a common subtype of idiopathic generalized epilepsy that shows a complex pattern of… 
2003
2003
Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy
Juvenile myoclonic epilepsy (JME) is a common subtype of idiopathic generalized epilepsy that shows a complex pattern of… 
2000
2000
Pathophysiology of KCNQ Channels: Neonatal Epilepsy and Progressive Deafness
Over the past 10 years, an increasing number of inherited diseases were shown to be due to mutations in ion channels. Given the… 
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