Evidence map›Paper›PMID 32509037›Full record

ArticleBehavioural neurology2020

A Novel PRRT2 Variant in Chinese Patients Suffering from Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsion.

Salem Baldi, Jin-Ling Zhu, Qing-Yun Hu, Ju-Li Wang, Jin-Bo Zhang, Shu-Hong Zhang

Open access · goldAbstract read
In one paragraph

Article in Behavioural neurology, 2020. 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
0.2field-weighted citation impact, top 52% 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, 3 citations in OpenAlex.

  1. 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 at 2 institutions in 1 country.

Salem BaldiDepartment of Biology, School of Basic Medicine, Jiamusi University, Jiamusi City, Heilongjiang Province, 154007, China.ORCID https://orcid.org/0000-0001-6711-1125
Jin-Ling ZhuDepartment of Biology, School of Basic Medicine, Jiamusi University, Jiamusi City, Heilongjiang Province, 154007, China.ORCID https://orcid.org/0000-0002-6978-147X
Qing-Yun HuDepartment of Anatomy, School of Basic Medicine, Jiamusi University, Jiamusi City, Heilongjiang Province, 154007, China.ORCID https://orcid.org/0000-0001-8287-4390
Ju-Li WangDepartment of Paediatrics, Central Hospital of Jiamusi, Jiamusi City Heilongjiang Province, 154002, China.ORCID https://orcid.org/0000-0002-9129-5478
Jin-Bo ZhangDepartment of Biology, School of Basic Medicine, Jiamusi University, Jiamusi City, Heilongjiang Province, 154007, China.ORCID https://orcid.org/0000-0001-6465-5426
Shu-Hong ZhangDepartment of Biology, School of Basic Medicine, Jiamusi University, Jiamusi City, Heilongjiang Province, 154007, China.ORCID https://orcid.org/0000-0002-3147-110X
Jiamusi University · CNFirst Affiliated Hospital of Jiamusi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PRRT2 mutations are the major causative agent of paroxysmal kinesigenic dyskinesia with infantile convulsion (PKD/IC). The study is aimed at screening PRRT2 gene mutations in patients who suffered from PKD/IC in Chinese population. Thirteen Chinese patients with PKD/IC were screened randomly for coding exons of the PRRT2 gene mutation along with 50 ethnically coordinated control people. Nine (2 unaffected) and 4 of the patients showed familial PKD/IC and apparently sporadic cases, respectively. We identified 5 different PRRT2 mutations in 10 individuals, including 8 familial and 2 apparently sporadic cases. However, no mutations were found in the 50 ethnically matched controls. Unknown (novel) NM_145239.2:c.686G>A and previously reported NM_145239.2:c.743G>C variants were identified in two familial and sporadic patients. All affected members of family A showed mutation NM_145239.2:c.650_670delinsCAATGGTGCCACCACTGGGTTA. The previously identified NM_145239.2:c.412 C>G and NM_145239.2:c.709G>A variants are seen in two individuals assessed in family B. Other than the previously identified variants, some of the patients with PRRT2-PKD/IC showed a new PRRT2 substitution variant. Thus, the spectrum of PRRT2 variants is expanded. The possible role and probability of PRRT2 variants involved in PKD/IC are highlighted.

Indexed as

ChoreaDystoniaEpilepsy, Benign NeonatalMembrane ProteinsNerve Tissue ProteinsChinaFemaleHumansMaleSeizuresMembrane ProteinsNerve Tissue ProteinsPRRT2 protein, human

Identifiers

PMID32509037
PMCPMC7251426
OpenAlexW3026145492

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.