Evidence map›Paper›PMID 36825575›Full record

ArticleMolecular medicine reports2023

A novel missense mutation in

Xing-Chen Wang, Rui-Han Liu, Ting Wang, Yanling Wang, Yan Jiang, Dan-Dan Chen, Xin-Yu Wang, Tong-Shu Hou, Qing-Xia Kong

Open access · hybridAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular medicine reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Eukaryotic translation initiation factorExperimental and therapeutic medicine · 2024
    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

9 authors at 4 institutions in 1 country.

Xing-Chen Wang *Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, P.R. China.
Rui-Han Liu *Department of Pediatrics, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, P.R. China.
Ting WangDepartment of Nursing, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, P.R. China.
Yanling WangDepartment of Nursing, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, P.R. China.
Yan JiangClinical Medical College, Jining Medical University, Jining, Shandong 272000, P.R. China.
Dan-Dan ChenClinical Medical College, Jining Medical University, Jining, Shandong 272000, P.R. China.
Xin-Yu WangClinical Medical College, Jining Medical University, Jining, Shandong 272000, P.R. China.
Tong-Shu HouSecond Clinical Medical College, Binzhou Medical University, Binzhou, Shandong 256600, P.R. China.
Qing-Xia KongCheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, P.R. China.
Affiliated Hospital of Jining Medical University · CNShandong University · CNJining Medical University · CNBinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary spastic paraplegia (HSP) comprises a group of hereditary and neurodegenerative diseases that are characterized by axonal degeneration or demyelination of bilateral corticospinal tracts in the spinal cord; affected patients exhibit progressive spasticity and weakness in the lower limbs. The most common manifestation of HSP is spastic paraplegia type 4 (SPG4), which is caused by mutations in the spastin (

Indexed as

Spastic Paraplegia, HereditaryHumansMaleMutationMutation, MissenseParaplegiaSpastinSpastinSPAST protein, humancase reporthereditary spastic paraplegianovel missense mutationspastic paraplegia type 4spastin

Identifiers

PMID36825575
PMCPMC10018243
OpenAlexW4321458313

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.