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

The lack of association between febrile convulsions and polymorphisms in SCN1A.

Epilepsy research - 1 Apr 2003

Chou I-Ching, Peng Ching-Tien, Tsai Fuu-Jen, Huang Chao-Ching, Shi Yi-Ru, Tsai Chang-Hai

Abstract excerpt

Febrile convulsions (FCs) represent the majority of childhood seizures, and patients have a genetic predisposition to their development. The genetic susceptibility to FCs seems to involve multiple genes in most instances. Recent studies provided evidence that mutations in SCN1A represent the most frequent cause of generalized epilepsy with febrile seizures plus an autosomal-dominant epilepsy syndrome. SCN1A...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Fever
Share to Genetic Markers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to NAV1.1 Voltage-Gated Sodium Channel

Share to Nerve Tissue Proteins

Share to Reverse Transcriptase Polymerase Chain Reaction

Share to Seizures

Share to Sodium Channels

Source

Identifiers

PMID: 12742596
DOI: 10.1016/s0920-1211(03)00043-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The lack of association between febrile convulsions and polymorphisms in SCN1A.PMID 12742596Read ↗

Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy.Semantic proximity Read ↗

Lack of replication of association between scn1a SNP and febrile seizures.Semantic proximity Read ↗

SCN1A rs3812718 polymorphism and susceptibility to epilepsy with febrile seizures: a meta-analysis.Semantic proximity Read ↗

Lack of SCN1A mutations in familial febrile seizures.Semantic proximity Read ↗

Replication of association between a SCN1A splice variant and febrile seizures.Semantic proximity Read ↗

Failure to find association between febrile seizures and SCN1A rs3812718 polymorphism in south Indian patients with mesial temporal lobe epilepsy and hippocampal sclerosis.Semantic proximity Read ↗

De-novo mutations and genetic variation in the SCN1A gene in Malaysian patients with generalized epilepsy with febrile seizures plus (GEFS+).Semantic proximity Read ↗

Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.Semantic proximity Read ↗

Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patients.Semantic proximity Read ↗

A novel SCN1A mutation in a cytoplasmic loop in intractable juvenile myoclonic epilepsy without febrile seizures.Semantic proximity Read ↗

A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.Semantic proximity Read ↗

Phenotypes and genotypes in epilepsy with febrile seizures plus.Semantic proximity Read ↗

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