Evidence map›Paper›PMID 34777470›Full record

ArticleFrontiers in genetics2021

Case Report: A Novel

Jie-Yuan Jin, Bing-Bing Guo, Yi Dong, Yue Sheng, Liang-Liang Fan, Li-Bing Zhang

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 90% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Therapeutic advances in neurological disorders · 2025
    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.

Jie-Yuan JinSchool of Life Sciences, Central South University, Changsha, China.
Bing-Bing GuoSchool of Life Sciences, Central South University, Changsha, China.
Yi DongSchool of Life Sciences, Central South University, Changsha, China.
Yue ShengSchool of Life Sciences, Central South University, Changsha, China.
Liang-Liang FanSchool of Life Sciences, Central South University, Changsha, China.
Li-Bing ZhangDepartment of Pediatrics, Affiliated Hospital of Yangzhou University, Yangzhou, China.
Central South University · CNYangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypokalemic periodic paralysis (HypoPP) is a rare autosomal dominant disorder characterized by episodic flaccid paralysis with concomitant hypokalemia. More than half of patients were associated with mutations in

Indexed as

CACNA1Scalcium channelsframeshift mutationhypokalaemic periodic paralysistargeted sequencing

Identifiers

PMID34777470
PMCPMC8586648
OpenAlexW3208562630

What OpenQuestion 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 OpenQuestion graph.