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

KCNJ10 gene mutation in an 8-year-old boy with seizures.

Acta neurologica Belgica - 1 Mar 2013

Kara Bülent, Ekici Barış, Ipekçi Belkıs, Aslanger Ayça Koçbaş, Scholl Ute

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Intellectual Disability
Share to Mutation
Share to Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Potassium Channels, Inwardly Rectifying

Share to Seizures

Source

Identifiers

PMID: 22782654
DOI: 10.1007/s13760-012-0113-2

Genes

KCNJ10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

KCNJ10 gene mutation in an 8-year-old boy with seizures.PMID 22782654Read ↗

KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr).Semantic proximity Read ↗

Novel Mutations in KCNJ10 Gene Associated With SeSAME Syndrome: Rare Disorder With Possible Common Mutation.Semantic proximity Read ↗

De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.Semantic proximity Read ↗

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological featuresSemantic proximity Read ↗

Mild phenotype in a patient with developmental and epileptic encephalopathy carrying a novel de novo KCNB1 variant.Semantic proximity Read ↗

MODY in China: two families carrying the KCNJ11 E229K variant.Semantic proximity Read ↗

Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene.Semantic proximity Read ↗

Contribution of KCNJ10 gene polymorphisms in childhood epilepsy.Semantic proximity Read ↗

Early glibenclamide treatment in a clinical newborn with KCNJ11 gene mutation.Semantic proximity Read ↗

Heterozygous KCNJ10 variants affecting Kir4.1 channel cause paroxysmal kinesigenic dyskinesiaSemantic proximity Read ↗

Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene.Semantic proximity Read ↗

An adult with KCNA2-related epilepsy and ataxia.Semantic proximity Read ↗

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