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Article

[Benign familial neonatal convulsions: molecular pathology and diagnosis].

Der Nervenarzt - 1 Aug 2000

Steinlein O K

Abstract excerpt

Benign familial neonatal convulsions are a rare monogenic form of idiopathic epilepsy characterized by the onset of frequent brief seizures after the second day of life. The seizures disappear spontaneously within a few weeks, but recurrent seizures later in life are common. Linkage studies located genes to chromosome 20q13.3 and 8q24, and the voltage-gated potassium channels KCNQ2 and KCNQ3 were recently...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10996911
DOI: 10.1007/s001150050637

Genes

KCNQ2
KCNQ3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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[Benign familial neonatal convulsions: molecular pathology and diagnosis].PMID 10996911Read ↗

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Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.Semantic proximity Read ↗

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Potassium channel genes and benign familial neonatal epilepsy.Semantic proximity Read ↗

[Clinical and genetic analysis of a Chinese pedigree affected with benign familial neonatal convulsion].Semantic proximity Read ↗

Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC).Semantic proximity Read ↗

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions.Semantic proximity Read ↗

Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels.Semantic proximity Read ↗

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.Semantic proximity Read ↗

[Benign familial neonatal convulsions: a model of idiopathic epilepsy].Semantic proximity Read ↗

The first Korean case of KCNQ2 mutation in a family with benign familial neonatal convulsions.Semantic proximity Read ↗

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