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

Novel DEPDC5 mutations causing familial focal epilepsy with variable foci identified.

Clinical genetics - 1 Oct 2013

Kaur A

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 Brain
Share to Epilepsies, Partial
Share to Exome
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Guanine Nucleotide Exchange Factors

Share to Mutation

Source

Identifiers

PMID: 23869883
DOI: 10.1111/cge.12239

Genes

DEPDC5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel DEPDC5 mutations causing familial focal epilepsy with variable foci identified.PMID 23869883Read ↗

Mutations in DEPDC5 cause familial focal epilepsy with variable foci.Semantic proximity Read ↗

Mutations of DEPDC5 cause autosomal dominant focal epilepsies.Semantic proximity Read ↗

Phenotypic and Genotypic Characterization of DEPDC5-Related Familial Focal Epilepsy: Case Series and Literature ReviewSemantic proximity Read ↗

A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French-Canadian population.Semantic proximity Read ↗

What is the impact of a novel DEPDC5 variant on an infant with focal epilepsy: a case report.Semantic proximity Read ↗

DEPDC5 plays a vital role in epilepsy: Genotypic and phenotypic features in cohort and literature.Semantic proximity Read ↗

DEPDC5 does it all: shared genetics for diverse epilepsy syndromes.Semantic proximity Read ↗

DEPDC5 mutations in familial and sporadic focal epilepsy.Semantic proximity Read ↗

DEPDC5 mutations in genetic focal epilepsies of childhood.Semantic proximity Read ↗

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy.Semantic proximity Read ↗

DEPDC5 takes a second hit in familial focal epilepsy.Semantic proximity Read ↗

Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.Semantic proximity Read ↗

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