Evidence map›Paper›PMID 30835075›Full record

ArticleCerebellum (London, England)2019

Correction to: Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital Ataxia.

Ginevra Zanni, P De Magistris, M Nardella, E Bellacchio, S Barresi, A Sferra, A Ciolfi, M Motta, H Lue, D Moreno-Andres and 3 more

Open access · bronzeAbstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 2 countries.

Ginevra ZanniDepartment of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy. ginevra.zanni@opbg.net.ORCID 0000-0002-6367-1843
P De MagistrisInstitute of Biochemistry and Molecular Cell Biology, Medical School, RWTH Aachen University, 52074, Aachen, Germany.
M NardellaDepartment of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.
E BellacchioGenetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
S BarresiGenetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
A SferraDepartment of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.
A CiolfiGenetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
M MottaGenetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
H LueInstitute of Biochemistry and Molecular Cell Biology, Medical School, RWTH Aachen University, 52074, Aachen, Germany.
D Moreno-AndresInstitute of Biochemistry and Molecular Cell Biology, Medical School, RWTH Aachen University, 52074, Aachen, Germany.
M TartagliaGenetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
E BertiniDepartment of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.
Wolfram AntoninInstitute of Biochemistry and Molecular Cell Biology, Medical School, RWTH Aachen University, 52074, Aachen, Germany. wantonin@ukaachen.de.
Bambino Gesù Children's Hospital · ITRWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The original version of this article unfortunately contained mistake in Fig. 3 image.

Identifiers

PMID30835075
OpenAlexW2918653417

What OpenQuestion holds

Textmetadata
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.