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Article

CLCN2 and idiopathic generalized epilepsy.

Advances in neurology - 1 Jan 2005

Heils Armin

Abstract excerpt

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Topics

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Share to Chloride Channels
Share to Epilepsy, Generalized
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15508929

Genes

CLCN2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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CLCN2 and idiopathic generalized epilepsy.PMID 15508929Read ↗

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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.Semantic proximity Read ↗

Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2Semantic proximity Read ↗

Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsySemantic proximity Read ↗

The KCC2 Cotransporter and Human Epilepsy: Getting Excited About Inhibition.Semantic proximity Read ↗

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[KCNQ2 gene mutations and neonatal epilepsy].Semantic proximity Read ↗

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