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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

1. DEPDC5-Related Familial Focal Epilepsy With Variable Foci-1: A Report of a Rare Case.Cureus · 2025
   Article
2. A Novel Loss-of-Function Mutation in the NPRL3 Gene Identified in Chinese Familial Focal Epilepsy with Variable Foci.Frontiers in genetics · 2021
   Article
3. DEPDC5 haploinsufficiency drives increased mTORC1 signaling and abnormal morphology in human iPSC-derived cortical neurons.Neurobiology of disease · 2020
   Article
4. Evaluation of magnetic resonance imaging-negative drug-resistant epilepsy.Annals of Indian Academy of Neurology · 2014
   Article

Corrections and comments

• Comment on
  Mutations in DEPDC5 cause familial focal epilepsy with variable foci.2013
• Comment on
  Mutations of DEPDC5 cause autosomal dominant focal epilepsies.2013

Authors and funding

1 author at 1 institution in 1 country.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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