Evidence map›Paper›PMID 33131365›Full record

ArticleThe Journal of international medical research2020

A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene.

Yue Wu, Jingzhe Han, Yaye Wang, Jinru Zhang, Xueqin Song, Guang Ji

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

Article in The Journal of international medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 84% 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, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
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

6 authors at 2 institutions in 1 country.

Yue WuDepartment of Neurology, The Second Hospital of Hebei Medical University, Hebei, Shijiazhuang, P. R. China.
Jingzhe HanDepartment of Neurology, Harrison International Peace Hospital, Hebei, Hengshui, P. R. China.ORCID https://orcid.org/0000-0002-6086-7533
Yaye WangDepartment of Neurology, The Second Hospital of Hebei Medical University, Hebei, Shijiazhuang, P. R. China.
Jinru ZhangDepartment of Neurology, The Second Hospital of Hebei Medical University, Hebei, Shijiazhuang, P. R. China.
Xueqin SongDepartment of Neurology, The Second Hospital of Hebei Medical University, Hebei, Shijiazhuang, P. R. China.ORCID https://orcid.org/0000-0003-0463-8450
Guang JiDepartment of Neurology, The Second Hospital of Hebei Medical University, Hebei, Shijiazhuang, P. R. China.
Hebei Medical University · CNHarrison International Peace Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a family with riboflavin-reactive multiple acyl-CoA dehydrogenase deficiency (RR-MADD) partially caused by a novel mutation in the electron transfer flavoprotein dehydrogenase gene

Indexed as

Electron-Transferring FlavoproteinsIron-Sulfur ProteinsMuscular DiseasesOxidoreductases Acting on CH-NH Group DonorsFemaleHumansLipidsMutationRiboflavinElectron-Transferring FlavoproteinsIron-Sulfur ProteinsLipidsOxidoreductases Acting on CH-NH Group DonorsRiboflavinelectromyographyETFDH genelipid depositionmuscle biopsymutationRiboflavin-reactive lipid deposition myopathy

Identifiers

PMID33131365
PMCPMC7653293
OpenAlexW3097558481

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.