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Article

DEPDC5 does it all: shared genetics for diverse epilepsy syndromes.

Annals of neurology - 1 May 2014

Poduri Annapurna

Abstract excerpt

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Topics

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Share to Brain
Share to Epilepsies, Partial
Share to Genetics and Neurodevelopmental Disorders
Share to GTPase-Activating Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intracellular Signaling Peptides and Proteins

Share to Mutation

Share to Repressor Proteins

Share to TOR Serine-Threonine Kinases

Source

Identifiers

PMID: 24753000
DOI: 10.1002/ana.24160

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→

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DEPDC5 does it all: shared genetics for diverse epilepsy syndromes.PMID 24753000Read ↗

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

Novel DEPDC5 mutations causing familial focal epilepsy with variable foci identified.Semantic proximity Read ↗

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 ↗

[Research progress on DEPDC5 gene related epilepsy].Semantic proximity Read ↗

De novo mutation in DEPDC5 associated with unilateral pachygyria and intractable epilepsy.Semantic proximity Read ↗

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

Clinical characteristics and genetic analysis of DEPDC5 gene variants related epilepsy in Chinese childrenSemantic proximity Read ↗

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

Expanding the Genotype and Phenotype of SETD5-Related Neurodevelopmental Syndrome.Semantic proximity Read ↗

Recent advances in epilepsy genomics and genetic testingSemantic proximity Read ↗

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