Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic basis of autosomal dominant nocturnal frontal lobe epilepsy.

Journal of applied genetics - 1 Jan 2003

Rózycka Agata, Trzeciak Wiesław H

Abstract excerpt

In this review the current literature regarding autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is presented and discussed. This disease is caused by mutations of genes coding for subunits of neuronal acetylcholine receptor comprising the sodium/potassium ion channel. To date, three types of mutations of the gene encoding alpha4 subunit of acetylcholine receptor were described in multi-generation...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Epilepsy, Frontal Lobe
Share to Family Health
Share to Frontal Lobe

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

Share to Genes, Dominant

Share to Ligands

Share to Receptors, Cholinergic

Share to Receptors, Nicotinic

Source

Identifiers

PMID: 12773798

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.

Related research

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic basis of autosomal dominant nocturnal frontal lobe epilepsy.PMID 12773798Read ↗

[Molecular and genetic basis of idiopathic nocturnal frontal lobe epilepsy].Semantic proximity Read ↗

Recent advances on autosomal dominant nocturnal frontal lobe epilepsy: "understanding the nicotinic acetylcholine receptor (nAChR)".Semantic proximity Read ↗

Autosomal dominant nocturnal frontal lobe epilepsy--a critical overview.Semantic proximity Read ↗

Autosomal dominant nocturnal frontal lobe epilepsy: an electroclinical study of a Norwegian family with ten affected members.Semantic proximity Read ↗

CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.Semantic proximity Read ↗

Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability.Semantic proximity Read ↗

Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family.Semantic proximity Read ↗

Genetic heterogeneity in familial nocturnal frontal lobe epilepsy.Semantic proximity Read ↗

Mutations in familial nocturnal frontal lobe epilepsy might be associated with distinct neurological phenotypes.Semantic proximity Read ↗

Dominant partial epilepsies. A clinical, electrophysiological and genetic study of 19 European families.Semantic proximity Read ↗

Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy.Semantic proximity Read ↗

How mutations in the nAChRs can cause ADNFLE epilepsy.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.