Evidence map›Paper›PMID 34925207›Full record

ArticleFrontiers in neurology2021

Two Novel Myelin Protein Zero Mutations in a Group of Chinese Patients.

Bin Chen, Zaiqiang Zhang, Na Chen, Wei Li, Hua Pan, Xingao Wang, Yuting Ren, Yuzhi Shi, Hongfei Tai, Songtao Niu

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

Article in Frontiers in neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

10 authors at 3 institutions in 1 country.

Bin ChenDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zaiqiang ZhangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Na ChenDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Wei LiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Hua PanDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Xingao WangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yuting RenDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yuzhi ShiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Hongfei TaiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Songtao NiuDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Beijing Tian Tan Hospital · CNCapital Medical University · CNNational Clinical Research Center for Digestive Diseases · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the myelin protein zero gene are responsible for the autosomal dominant Charcot-Marie-Tooth disease (CMT). We summarized the genetic and clinical features of six unrelated Chinese families and the genetic spectrum of Chinese patients with myelin protein zero (

Indexed as

Charcot-Marie-Tooth diseaseChineseJapaneseKoreansmyelin protein zerospectrum

Identifiers

PMID34925207
PMCPMC8674198
OpenAlexW3216536331

What OpenQuestion holds

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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.