KCNT1 gene

Known as: KCNT1, KIAA1422, potassium sodium-activated channel subfamily T member 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2012-2018
051020122018

Papers overview

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2016
2016
OBJECTIVES We report development of a targeted resequencing gene panel for focal epilepsy, the most prevalent phenotypic group of… (More)
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2015
2015
We report 2 patients with drug-resistant epilepsy caused by KCNT1 mutations who were treated with quinidine. Both mutations… (More)
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2015
2015
Autosomal dominant mutations in the sodium-gated potassium channel subunit gene KCNT1 have been associated with two distinct… (More)
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2015
2015
KCNT1 mutations have been found in epilepsy of infancy with migrating focal seizures (EIMFS; also known as migrating partial… (More)
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2014
2014
Migrating partial seizures of infancy is an early onset epileptic encephalopathy syndrome that is typically resistant to… (More)
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2014
2014
In severe early-onset epilepsy, precise clinical and molecular genetic diagnosis is complex, as many metabolic and electro… (More)
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2014
2014
BACKGROUND More than half of patients with genetic leukoencephalopathies remain without a specific diagnosis; this is… (More)
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2013
2013
We performed analysis of KCNT1 in two unrelated patients with malignant migrating partial seizures in infancy. Both patients had… (More)
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Highly Cited
2012
Highly Cited
2012
We performed genomic mapping of a family with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) and intellectual and… (More)
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2012
2012
Slick and Slack high-conductance potassium channels have been recently discovered, and are found in the central nervous system… (More)
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