Evidence map›Paper›PMID 28091420›Full record

ArticleChinese medical journal2017

Compound Heterozygote Mutation of

Xiao-Jing Fang, Wei Zhang, He Lyu, Zhao-Xia Wang, Wei-Wei Wang, Yun Yuan

Open access · greenAbstract readCase Reports
In one paragraph

Article in Chinese medical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. [Combined oxidative phosphorylation deficiency type 7 caused byZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Review
  4. Review
  5. Article
  6. [Clinical features and C12orf65 mutations of autosomal recessive spastic paraplegia-55: a case report].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2019
    Article
  7. Article
  8. 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

6 authors at 2 institutions in 1 country.

Xiao-Jing FangDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Wei ZhangDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
He LyuDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Zhao-Xia WangDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Wei-Wei WangDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Yun YuanDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Peking University · CNPeking University First Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ChildFemaleHereditary Sensory and Motor NeuropathyHeterozygoteHumansMitochondrial ProteinsMutationOptic AtrophyPeptide Termination FactorsMitochondrial ProteinsMTRFR protein, humanPeptide Termination Factors

Identifiers

PMID28091420
PMCPMC5282685
OpenAlexW2572024980

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.