Genetics: expanding the spectrum of neurological disorders associated with PRRT2 mutations.

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.

1. Genetic and epigenetic mechanisms of epilepsy: a review.Neuropsychiatric disease and treatment · 2017
   Review
2. A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE.The Journal of biological chemistry · 2016
   Article
3. A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology.American journal of human genetics · 2015
   Article
4. Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.Molecular genetics & genomic medicine · 2013
   Article

Corrections and comments

• Comment on
  PRRT2 mutations cause hemiplegic migraine.2012
• Comment on
  PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures.2012
• Comment on
  PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.2012
• Comment on
  PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.2012

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.