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

Juvenile myoclonic epilepsy is not associated with the DRPLA gene in a European population.

In vivo (Athens, Greece) - 1 Jan 2000

Yapijakis Christos, Gatzonis Stergios, Youroukos Sotirios, Kollia Vasiliki, Karachristianou Stella, Anagnostouli Maria

Abstract excerpt

BACKGROUND: Juvenile myoclonic epilepsy (JME), is an early-onset inherited generalized epilepsy which displays genetic heterogeneity, with at least 10 known loci. Another neurogenetic disease, dentato-rubro-pallido-luysian atrophy (DRPLA) presents three clinical phenotypes, one of which in Japanese displays many similarities to JME. AIM: The purpose of this study was to investigate whether the DRPLA gene is...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myoclonic Epilepsy, Juvenile

Share to Nerve Tissue Proteins

Share to Polymorphism, Genetic

Share to Trinucleotide Repeats

Share to White People

Share to Young Adult

Source

Identifiers

PMID: 25398822

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

Juvenile myoclonic epilepsy is not associated with the DRPLA gene in a European population.PMID 25398822Read ↗

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.Semantic proximity Read ↗

Clinical genetic study in juvenile myoclonic epilepsy.Semantic proximity Read ↗

Clinical characteristics of a South Indian cohort of juvenile myoclonic epilepsy probands.Semantic proximity Read ↗

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

Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.Semantic proximity Read ↗

The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy.Semantic proximity Read ↗

Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.Semantic proximity Read ↗

Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.Semantic proximity Read ↗

Association analysis of a regulatory promoter polymorphism of the PAX-6 gene with idiopathic generalized epilepsy.Semantic proximity Read ↗

Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsy.Semantic proximity Read ↗

Sporadic cases of dentatorubral-pallidoluysian atrophy associated with maternal transmission.Semantic proximity Read ↗

Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy.Semantic proximity Read ↗

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