Evidence map›Paper›PMID 42527655›Full record

ArticleEMBO molecular medicine2026

Author Correction: Domain-substituted IGF2 tag modulates targeting of lentiviral gene therapy for Hunter syndrome.

Fabio Catalano, Dejan Stevic, Giacomo Zundo, Tessa F Huizer, Zina Dammou, Eva C Vlaar, Drosos Katsavelis, Jeroen C van den Bosch, Hannerieke J M P van den Hout, Esmeralda Oussoren and 4 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in EMBO molecular medicine, 2026. 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

14 authors.

Fabio CatalanoDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands. f.catalano@erasmusmc.nl.
Dejan Stevic *Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.ORCID http://orcid.org/0009-0009-0837-1993
Giacomo Zundo *Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Tessa F HuizerDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Zina DammouDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Eva C VlaarDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Drosos KatsavelisDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.ORCID http://orcid.org/0000-0001-6841-2210
Jeroen C van den BoschDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Hannerieke J M P van den HoutDepartment of Pediatrics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Esmeralda OussorenDepartment of Pediatrics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Ans T van der PloegDepartment of Pediatrics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
George J G RuijterDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
Gerben SchaafDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands.
W W M Pim PijnappelDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, 3015GE, The Netherlands. w.pijnappel@erasmusmc.nl.ORCID http://orcid.org/0000-0002-7042-2482

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID42527655
PMCPMC13562546

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.