Evidence map›Paper›PMID 40443206›Full record

ArticleMovement disorders clinical practice2025

Novel VAC14 Variants Identified in a Patient with Striatonigral Degeneration and Prolonged Survival.

Silvestre Cuinat, Christèle Dubourg, Gaël Nicolas, Jean-Madeleine de Sainte Agathe, Sylvie Odent, Laurent Pasquier, Audrey Riou

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Movement disorders clinical practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Silvestre CuinatService de Génétique Clinique, CRMR anomalies du développement CLAD-Ouest, CRDI (Centre de Référence Déficiences Intellectuelles de Causes Rares), CHU Rennes, Rennes, France.ORCID https://orcid.org/0000-0002-0763-5661
Christèle DubourgLaboratoire de Génétique Moléculaire, Hôpital Pontchaillou, CHU Rennes, Rennes, France.
Gaël NicolasDepartment of Genetics, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, France.
Jean-Madeleine de Sainte AgatheLBM SeqOIA, Paris, France.
Sylvie OdentService de Génétique Clinique, CRMR anomalies du développement CLAD-Ouest, CRDI (Centre de Référence Déficiences Intellectuelles de Causes Rares), CHU Rennes, Rennes, France.
Laurent PasquierService de Génétique Clinique, CRMR anomalies du développement CLAD-Ouest, CRDI (Centre de Référence Déficiences Intellectuelles de Causes Rares), CHU Rennes, Rennes, France.
Audrey RiouService de Génétique Clinique, CRMR anomalies du développement CLAD-Ouest, CRDI (Centre de Référence Déficiences Intellectuelles de Causes Rares), CHU Rennes, Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

dystonianeurodegeneration with brain iron accumulationspastic tetraplegiastriatonigral degenerationVAC14

Identifiers

PMID40443206
PMCPMC12528970

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.