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

[Association between SCN1A rs3812718 polymorphism and generalized epilepsy with febrile seizures plus].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 Feb 2018

Ma Qi-Ling, Wang Bo, Chen Guang-Fu, Huang Jian-Lin, Li Yun, Cao De-Zhi, Liu Rong-Tian

Abstract excerpt

OBJECTIVE: To investigate the association between SCN1A rs3812718 polymorphism and generalized epilepsy with febrile seizures plus (GEFS+), and to provide potential molecular targets for the diagnosis and treatment of GEFS+. METHODS: The iPLEX technique in the MassARRAY system was used to determine SCN1A rs3812718 polymorphism, genotype frequency, and allele frequency in 50 patients with GEFS+ and 50 healthy...

Read the complete abstract on PubMed

Topics

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Adolescent
Share to Child
Share to Child, Preschool
Share to Epilepsy, Generalized
Share to Genotype
Share to NAV1.1 Voltage-Gated Sodium Channel
Share to Polymorphism, Single Nucleotide
Share to Seizures, Febrile

Source

Open in PubMed Open full text

Identifiers

PMID: 29429462
PMCID: PMC7389242

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Association between SCN1A rs3812718 polymorphism and generalized epilepsy with febrile seizures plus].PMID 29429462Read ↗

[Clinical analysis and screening for SCN1A gene mutation in two pedigrees of generalized epilepsies with febrile seizures plus].Semantic proximity Read ↗

[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].Semantic proximity Read ↗

[Analysis of clinical phenotype and SCN1A gene variant in a pedigree affected with genetic epilepsy with febrile seizures].Semantic proximity Read ↗

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.Semantic proximity Read ↗

Novel mutation of SCN9A gene causing generalized epilepsy with febrile seizures plus in a Chinese family.Semantic proximity Read ↗

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

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

Novel mutation of SCN1A in familial generalized epilepsy with febrile seizures plus.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 ↗

SCN1A rs3812718 polymorphism is associated with epilepsy: An updated meta-analysis.Semantic proximity Read ↗

Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+).Semantic proximity Read ↗

Mutation screening of three Chinese families with genetic epilepsy with febrile seizures plus.Semantic proximity Read ↗

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