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Article

Mesial temporal lobe epilepsy associated with KCNT1 mutation.

Seizure - 1 Feb 2017

Hansen N, Widman G, Hattingen E, Elger C E, Kunz W S

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28081520
DOI: 10.1016/j.seizure.2016.12.018

Genes

KCNT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mesial temporal lobe epilepsy associated with KCNT1 mutation.PMID 28081520Read ↗

KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects.Semantic proximity Read ↗

Epilepsy of infancy with migrating focal seizures due to a novel homozygous mutation in KCNT1 gene: A case report.Semantic proximity Read ↗

Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy.Semantic proximity Read ↗

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsySemantic proximity Read ↗

A novel KCNT1 mutation in a Chinese family with severe autosomal-dominant nocturnal frontal lobe epilepsySemantic proximity Read ↗

Characteristics of epilepsy in patients with Kabuki syndrome with KMT2D mutations.Semantic proximity Read ↗

Functional Effects of Epilepsy Associated KCNT1 Mutations Suggest Pathogenesis via Aberrant Inhibitory Neuronal Activity.Semantic proximity Read ↗

Identification of a novel de novo p.Phe932Ile KCNT1 mutation in a patient with leukoencephalopathy and severe epilepsy.Semantic proximity Read ↗

Efficacy of ethosuximide on atonic seizures with KCNB1 mutation.Semantic proximity Read ↗

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutationSemantic proximity Read ↗

Epilepsy: Genetic variant in subtype of MTLE.Semantic proximity Read ↗

An adult with KCNA2-related epilepsy and ataxia.Semantic proximity Read ↗

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