- 1Department of Pediatric Hematology, Emma Children’s Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands
- 2Department of Hematology, Erasmus University Medical Centre, Rotterdam, Netherlands
- 3Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam University Medical Centre, Amsterdam, Netherlands
- 4Division of Thrombosis and Hemostasis, Department of Internal Medicine, Leiden University Medical Centre, Leiden, Netherlands
A Correction on
Rewriting the script: gene therapy and genome editing for von Willebrand Disease
by Barraclough A, Bär I, van Duijl T, Fijnvandraat K, Eikenboom JCJ, Leebeek FWG, Bierings R, Voorberg J and Trasanidou D (2025). Front. Genome Ed. 7:1620438. doi: 10.3389/fgeed.2025.1620438
There was a mistake in the caption of Figure 1 as published. The legend of Figure 1 included text from an older version of the figure, which should have been removed. The incorrect caption read: Overview of von Willebrand Disease sub-types, von Willbrand Factor (VWF) domains, and variant distributions. (A) Summary of von Willebrand Disease sub-types (A) Von Willebrand Factor domains and binding sites. (B) Distribution and frequency of von Willebrand Factor variants curated in the Leiden Open Variation Database (LOVD) (Accessed and data retrieved on 8-1-2025). Created in BioRender.
The corrected caption of Figure 1 appears below.
Overview of von Willbrand Factor (VWF) domains, and variant distributions. (A) Von Willebrand Factor domains and binding sites. (B) Distribution and frequency of von Willebrand Factor variants curated in the Leiden Open Variation Database (LOVD) (Accessed and data retrieved on 8-1-2025). Created in BioRender.
The original article has been updated.
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Keywords: gene therapy, VWD, endothelial cells, delivery, CRISPR-Cas, in vivo delivery
Citation: Barraclough A, Bär I, van Duijl T, Fijnvandraat K, Eikenboom JCJ, Leebeek FWG, Bierings R, Voorberg J and Trasanidou D (2025) Correction: Rewriting the script: gene therapy and genome editing for von Willebrand Disease. Front. Genome Ed. 7:1719330. doi: 10.3389/fgeed.2025.1719330
Received: 06 October 2025; Accepted: 17 October 2025;
Published: 07 November 2025.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2025 Barraclough, Bär, van Duijl, Fijnvandraat, Eikenboom, Leebeek, Bierings, Voorberg and Trasanidou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jan Voorberg, ai52b29yYmVyZ0BzYW5xdWluLm5s
†These authors have contributed equally to this work
Jeroen C. J. Eikenboom4