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

[KCNQ2 gene mutations and neonatal epilepsy].

Medicina clinica - 24 Dec 2021

García Castellanos María Teresa, López Pisón Javier, Pérez Delgado Raquel

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 Epilepsy
Share to Infant, Newborn
Share to KCNQ2 Potassium Channel
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33962768
DOI: 10.1016/j.medcli.2021.01.019

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

[KCNQ2 gene mutations and neonatal epilepsy].PMID 33962768Read ↗

Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness.Semantic proximity Read ↗

Biallelic variants of KCNQ2 in early infantile developmental and epileptic encephalopathy.Semantic proximity Read ↗

Nine patients with KCNQ2-related neonatal seizures and functional studies of two missense variants.Semantic proximity Read ↗

[Benign familial neonatal convulsions: molecular pathology and diagnosis].Semantic proximity Read ↗

KCNQ2 Epileptic Encephalopathy in Early Infancy.Semantic proximity Read ↗

[Genotype and phenotype of children with KCNA2 gene related developmental and epileptic encephalopathy].Semantic proximity Read ↗

Potassium channel genes and benign familial neonatal epilepsy.Semantic proximity Read ↗

KCNQ2 related-epilepsy: Report of nine cases and novel loss-of-function missense variantsSemantic proximity Read ↗

KCNQ2, the first gene found to be mutated in human generalized idiopathic epilepsy.Semantic proximity Read ↗

KCNQ2-Associated Epilepsy: A Review of Variable Phenotypes and Neurodevelopmental OutcomesSemantic proximity Read ↗

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.Semantic proximity Read ↗

KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization.Semantic proximity Read ↗

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