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. 2024 Oct 7;19:369. doi: 10.1186/s13023-024-03296-6

Correction to: Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA

Nicole Revencu 1,#, Astrid Eijkelenboom 2,#, Claire Bracquemart 3,#, Pia Alhopuro 4, Judith Armstrong 5, Eulalia Baselga 6, Claudia Cesario 7, Maria Lisa Dentici 8, Melanie Eyries 9, Sofia Frisk 10, Helena Gásdal Karstensen 11, Nagore Gene‑Olaciregui 12, Sirpa Kivirikko 13, Cinzia Lavarino 12, Inger‑Lise Mero 14, Rodolphe Michiels 1, Elisa Pisaneschi 15, Bitten Schönewolf‑Greulich 11, Ilse Wieland 16, Martin Zenker 16,#, Miikka Vikkula 17,18,19,✉,#
PMCID: PMC11459908  PMID: 39375751

Correction to: Revencu et al. Orphanet Journal of Rare Diseases

10.1186/s13023-024-03196-9

Following publication of the original article [1], we have been notified that there was a mistake in supplementary and additional materials’ references.

It should be as per below:

Supplementary file 1 contains Table S1

Supplementary file 2 contains Additional file 1: Curations of each gene–disease asso­ciation

Supplementary file 3 contains Table S2

Supplementary file 4 contains Table S3

Footnotes

The online version of the original article can be found at 10.1186/s13023-024-03196-9.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Nicole Revencu, Astrid Eijkelenboom and Claire Bracquemart contributed equally to this work.

Martin Zenker and Miikka Vikkula contributed equally to this work.

Reference

  • 1.Revencu et al. (2024) Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA (2024). 19:213 10.1186/s13023-024-03196-9 [DOI] [PMC free article] [PubMed]

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