KCNC3 gene

Known as: Kv3.3, POTASSIUM CHANNEL, VOLTAGE-GATED, SHAW-RELATED SUBFAMILY, MEMBER 3, KCNC3 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2015
01219922015

Papers overview

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2015
2015
Spinocerebellar ataxia type 13 (SCA13) is an autosomal dominantly inherited neurodegenerative disorder of the cerebellum caused… (More)
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2014
2014
Spinocerebellar ataxia 13 (SCA13) is an autosomal dominant disease resulting from mutations in KCNC3 (Kv3.3), a voltage-gated… (More)
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2013
2013
The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of neurodegenerative disorders, among… (More)
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Review
2012
Review
2012
In this issue of Annals of Neurology, Duarri et al 1 and Lee et al report the identification of a gene that when mutated causes a… (More)
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2011
2011
BACKGROUND Gain-of function or dominant-negative mutations in the voltage-gated potassium channel KCNC3 (Kv3.3) were recently… (More)
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2009
2009
The role of cerebellar Kv3.1 and Kv3.3 channels in motor coordination was examined with an emphasis on the deep cerebellar nuclei… (More)
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2008
2008
The fast-activating/deactivating voltage-gated potassium channel Kv3.3 (Kcnc3) is expressed in various neuronal cell types… (More)
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2008
2008
Spinocerebellar ataxia 13 (SCA13), initially described in a four-generation French family, has now also been characterized in a… (More)
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Highly Cited
2006
Highly Cited
2006
Potassium channel mutations have been described in episodic neurological diseases. We report that K+ channel mutations cause… (More)
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1992
1992
Genomic and cDNA clones encoding a novel Shaw-related potassium channel gene have been isolated from mice and humans. The mouse… (More)
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