Evidence map›Paper›PMID 37668947›Full record

ArticleActa neurologica Belgica2024

A novel DCTN1 mutation causing perry syndrome leads to abnormal splicing of mRNA: genetic and functional analyses.

Wotu Tian, Li Yao, Guochao Shi, Ranran Dai, Li Cao

Open access · hybridAbstract readLetter
In one paragraph

Article in Acta neurologica Belgica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 27% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

5 authors at 1 institution in 1 country.

Wotu Tian *Department of Neurology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, China.
Li Yao *Department of Neurology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, China.
Guochao ShiDepartment of Respiratory and Critical Care Medicine, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
Ranran DaiDepartment of Respiratory and Critical Care Medicine, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China. drr11154@rjh.com.cn.
Li CaoDepartment of Neurology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, China. caoli2000@yeah.net.ORCID http://orcid.org/0000-0003-1742-9877
Shanghai Jiao Tong University · CN

Funding

China Postdoctoral Science Foundation No. 2022M712117Leading Talents in Health Care of Shanghai Municipal Health Commission No. 2022LJ011National Natural Science Foundation for Young Scholars of China No. 82201398Science and Technology Commission of Shanghai Municipality No. 23XD1402500Shanghai Pujiang Program No.22PJD052the National Natural Science Foundation of China No. 82071258Young Scholar Cultivation Project of Basic Scientific Research in Shanghai Sixth People's Hospital No. YNQN202224
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HypoventilationParkinsonian DisordersTDP-43 ProteinopathiesDepressionDynactin ComplexHumansMutationRNA, MessengerDCTN1 protein, humanDynactin ComplexRNA, MessengerDepressionHypoventilationInsomniaParkinsonismPerry syndrome

Identifiers

PMID37668947
PMCPMC10965570
OpenAlexW4386438254

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.