Evidence map›Paper›PMID 30647958›Full record

ArticleJournal of ophthalmology2018

Corrigendum to "Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles".

Smaragda Kamakari, Vassiliki Kokkinou, George Koutsodontis, Polixeni Stamatiou, Christoforos Giatzakis, Anastasios Anastasakis, Ioannis Minas Aslanides, Stavrenia Koukoula, Theoni Panagiotoglou, Ioannis Datseris and 1 more

Abstract readPublished Erratum
In one paragraph

Article in Journal of ophthalmology, 2018. 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
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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Smaragda KamakariOphthalmic Genetics Unit, OMMA Ophthalmological Institute of Athens, Athens, Greece.ORCID 0000-0003-4723-5213
Vassiliki KokkinouOphthalmic Genetics Unit, OMMA Ophthalmological Institute of Athens, Athens, Greece.
George KoutsodontisOphthalmic Genetics Unit, OMMA Ophthalmological Institute of Athens, Athens, Greece.
Polixeni StamatiouOphthalmic Genetics Unit, OMMA Ophthalmological Institute of Athens, Athens, Greece.
Christoforos GiatzakisDNAbiolab, Cretan Center for Research and Development of Applications on Genetics and Molecular Biology, Heraklion, Crete, Greece.
Anastasios AnastasakisDepartment of Clinical Electrophysiology of Vision, Athens Eye Hospital, Glyfada, Athens, Greece.ORCID 0000-0001-7526-7832
Ioannis Minas AslanidesDepartment of Ophthalmology, Emmetropia Mediterranean Eye Institute, Heraklion, Crete, Greece.
Stavrenia KoukoulaOphthalmica Institute of Ophthalmology and Microsurgery, Thessaloniki, Greece.
Theoni PanagiotoglouDepartment of Ophthalmology, University of Crete School of Medicine, Heraklion, Greece.ORCID 0000-0003-3553-1779
Ioannis DatserisDepartment of Retinal Disorders, OMMA Ophthalmological Institute of Athens, Athens, Greece.
Miltiadis K TsilimbarisDepartment of Ophthalmology, University of Crete School of Medicine, Heraklion, Greece.ORCID 0000-0002-0130-1150

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.1155/2018/5706142.].

Identifiers

PMID30647958
PMCPMC6311797

What OpenQuestion holds

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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.