Orphanet Journal of Rare Diseases (Oct 2024)
Correction to: Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA
- Nicole Revencu,
- Astrid Eijkelenboom,
- Claire Bracquemart,
- Pia Alhopuro,
- Judith Armstrong,
- Eulalia Baselga,
- Claudia Cesario,
- Maria Lisa Dentici,
- Melanie Eyries,
- Sofia Frisk,
- Helena Gásdal Karstensen,
- Nagore Gene‑Olaciregui,
- Sirpa Kivirikko,
- Cinzia Lavarino,
- Inger‑Lise Mero,
- Rodolphe Michiels,
- Elisa Pisaneschi,
- Bitten Schönewolf‑Greulich,
- Ilse Wieland,
- Martin Zenker,
- Miikka Vikkula
Affiliations
- Nicole Revencu
- Center for Human Genetics, Cliniques universitaires Saint-Luc, University of Louvain, VASCERN VASCA European Reference Centre
- Astrid Eijkelenboom
- Department of Pathology, Radboud University Medical Center, VASCERN VASCA European Reference Centre
- Claire Bracquemart
- Normandie Univ, UNICAEN, Service de Génétique, CHU Caen Normandie, VASCERN VASCA European Reference Centre
- Pia Alhopuro
- HUS Diagnostic Center, Laboratory of Genetics, University of Helsinki and Helsinki University Hospital, VASCERN VASCA European Reference Centre
- Judith Armstrong
- Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, CIBER‑ER (Biomedical Network Research Center for Rare Diseases), Instituto de Salud Carlos III (ISCIII), Madrid, and Genomic Unit, Molecular and Genetic Medicine Section, Hospital Sant Joan de Déu, VASCERN VASCA European Reference Centre
- Eulalia Baselga
- Department of Dermatology, Hospital Sant Joan de Deu, VASCERN VASCA European Reference Centre
- Claudia Cesario
- Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital and Research Institute, IRCCS, VASCERN VASCA European Reference Centre
- Maria Lisa Dentici
- Medical Genetics Unit, Bambino Gesù Children’s Hospital, IRCCS, VASCERN VASCA European Reference Centre
- Melanie Eyries
- Sorbonne Université, Département de Génétique, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié- Salpêtrière, VASCERN VASCA European Reference Centre
- Sofia Frisk
- Department of Molecular Medicine and Surgery, Karolinska Institutet, Department of Clinical Genetics, Karolinska University Hospital, VASCERN VASCA European Reference Centre
- Helena Gásdal Karstensen
- Department of Genetics, Center of Diagnostics, Copenhagen University Hospital - Rigshospitalet, VASCERN VASCA European Reference Centre
- Nagore Gene‑Olaciregui
- Laboratory of Molecular Oncology, Pediatric Cancer Center Barcelona, Hospital Sant Joan de Déu, VASCERN VASCA European Reference Centre
- Sirpa Kivirikko
- Department of Clinical Genetics, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, VASCERN VASCA European Reference Centre
- Cinzia Lavarino
- Laboratory of Molecular Oncology, Pediatric Cancer Center Barcelona, Hospital Sant Joan de Déu, VASCERN VASCA European Reference Centre
- Inger‑Lise Mero
- Department of Medical Genetics, Oslo University Hospital, VASCERN VASCA European Reference Centre
- Rodolphe Michiels
- Center for Human Genetics, Cliniques universitaires Saint-Luc, University of Louvain, VASCERN VASCA European Reference Centre
- Elisa Pisaneschi
- Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital and Research Institute, IRCCS, VASCERN VASCA European Reference Centre
- Bitten Schönewolf‑Greulich
- Department of Genetics, Center of Diagnostics, Copenhagen University Hospital - Rigshospitalet, VASCERN VASCA European Reference Centre
- Ilse Wieland
- Institute of Human Genetics, University Hospital Otto-Von-Guericke-University
- Martin Zenker
- Institute of Human Genetics, University Hospital Otto-Von-Guericke-University
- Miikka Vikkula
- Center for Vascular Anomalies, Cliniques Universitaires Saint-Luc
- DOI
- https://doi.org/10.1186/s13023-024-03296-6
- Journal volume & issue
-
Vol. 19,
no. 1
pp. 1 – 2
Abstract
No abstracts available.