Evidence map›Paper›PMID 34457282›Full record

ArticleClinical case reports2021

Report of a novel missense mutation in the

Maria Arvio, Maria Haanpää, Pia Pohjola, Jaana Lähdetie

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 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
0.3field-weighted citation impact, top 33% 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, 3 citations in OpenAlex.

  1. Article
  2. Broadening the Phenotype Spectrum of MECP2 Variants in Men.Molecular genetics & genomic medicine · 2025
    Article
  3. Report of a novel missense mutation in theClinical case reports · 2021
    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

4 authors at 3 institutions in 1 country.

Maria ArvioNeurology Päijät-Häme Joint Municipal Authority Lahti Finland.ORCID https://orcid.org/0000-0002-2571-7118
Maria HaanpääDepartment of Genomics Turku University Hospital Turku Finland.ORCID https://orcid.org/0000-0003-3731-863X
Pia PohjolaDepartment of Genomics Turku University Hospital Turku Finland.
Jaana LähdetieDepartment of Child Neurology Turku University Hospital Turku Finland.
Turku University Hospital · FIOulu University Hospital · FIUniversity of Turku · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exome sequencing revealed the cause of our 35-year-old male patient's progressive and severe intellectual and motor disability, namely a previously undescribed missense mutation of MECP2.

Indexed as

intellectual disabilityMECP2movement disorderprogressive disorder

Identifiers

PMID34457282
PMCPMC8380086
OpenAlexW3194063137

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.