Evidence map›Paper›PMID 32328026›Full record

ArticleFrontiers in neurology2020

Novel NtA and LG1 Mutations in Agrin in a Single Patient Causes Congenital Myasthenic Syndrome.

Aiping Wang, Yangyang Xiao, Peng Huang, Lingjuan Liu, Jie Xiong, Jian Li, Ding'an Mao, Liqun Liu

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

Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Aiping WangDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Yangyang XiaoDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Peng HuangDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Lingjuan LiuDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Jie XiongDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Jian LiDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Ding'an MaoDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Liqun LiuDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital myasthenic syndrome (CMS) is a group of genetic disorders of neuromuscular transmission that is characterized by muscle weakness. A mutation in the gene encoding agrin (

Indexed as

agrinAGRNcongenital myasthenic syndromemissense mutationwhole-exome sequencing

Identifiers

PMID32328026
PMCPMC7160337
OpenAlexW3015469972

What OpenQuestion holds

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LicenceCC BY
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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.