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

Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.

Epilepsy research - 1 Sept 2013

Manna Ida, Labate Angelo, Mumoli Laura, Ferlazzo Edoardo, Aguglia Umberto, Quattrone Aldo, Gambardella Antonio

Abstract excerpt

A recent study has implicated a tagging single nucleotide polymorphism (SNP) rs398702 located 3' of KCNMB4 (encoding calcium-activated potassium channel, subfamily M subunit beta 4) as a possible susceptibility allele for mesial temporal lobe epilepsy (mTLE). Such a finding warrants a further well-powered study in additional carefully phenotyped cohorts. Here we examined the role of the SNP (rs398702) in a cohort...

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 Anticonvulsants

Share to Electroencephalography

Share to Epilepsy, Temporal Lobe

Share to Hippocampus

Share to Magnetic Resonance Imaging

Share to Reproducibility of Results

Share to Sclerosis

Source

Identifiers

PMID: 23623847
DOI: 10.1016/j.eplepsyres.2013.03.014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.PMID 23623847Read ↗

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 ↗

No association between polymorphisms in the calcium homeostasis modulator 1 gene and mesial temporal lobe epilepsy risk in a Chinese population.Semantic proximity Read ↗

GABABR1 (G1465A) gene variation and temporal lobe epilepsy controversy: new evidence.Semantic proximity Read ↗

Lack of association between synapsin II (SYN2) gene polymorphism and susceptibility epilepsy: a case-control study and meta-analysis.Semantic proximity Read ↗

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

Lack of pathogenic mutations in six patients with MMPSI.Semantic proximity Read ↗

Lack of association between temporal lobe epilepsy and a novel polymorphism in the alpha 2 subunit gene (ATP1A2) of the sodium potassium transporting ATPase.Semantic proximity Read ↗

Failure to confirm association between RGS4 haplotypes and schizophrenia in Caucasians.Semantic proximity Read ↗

Major vault protein (MVP) gene polymorphisms and drug resistance in mesial temporal lobe epilepsy with hippocampal sclerosis.Semantic proximity Read ↗

Lack of association between rs211037 of the GABRG2 gene and juvenile myoclonic epilepsy in Brazilian population.Semantic proximity Read ↗

SLC6A4 gene variants and temporal lobe epilepsy susceptibility: a meta-analysis.Semantic proximity Read ↗

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

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