Evidence map›Paper›PMID 29451154›Full record

ArticleChinese medical journal2018

Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis.

Yang-Qi Xu, Xiao-Li Liu, Xiao-Jun Huang, Wo-Tu Tian, Hui-Dong Tang, Li Cao

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Chinese medical journal, 2018. 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
–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

2 citing papers in PubMed.

  1. New phenotype of severe neonatal episodic laryngospasm due to a missense mutation in SCN4A: A case report and literature review.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2021
    Review
  2. 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.

Yang-Qi XuDepartment of Neurology, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai 200025, China.
Xiao-Li LiuDepartment of Neurology, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai 200025; Department of Neurology, Shanghai Fengxian District Central Hospital, Shanghai Jiao Tong University Affiliated Sixth People's Hospital South Campus, Shanghai 201499, China.
Xiao-Jun HuangDepartment of Neurology, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai 200025; Department of Neurology, Ruijin Hospital North, Shanghai Jiao Tong University, Shanghai 201800, China.
Wo-Tu TianDepartment of Neurology, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai 200025, China.
Hui-Dong TangDepartment of Neurology, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai 200025, China.
Li CaoDepartment of Neurology, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai 200025, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationChloride ChannelsHumansMyotonia CongenitaNAV1.4 Voltage-Gated Sodium ChannelScoliosisChloride ChannelsNAV1.4 Voltage-Gated Sodium ChannelSCN4A protein, human

Identifiers

PMID29451154
PMCPMC5830834

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.