Correction to: European Journal of Human Genetics https://doi.org/10.1038/s41431-024-01664-1, published online 12 July 2024
There was an error in the labeling of Table 1.
The values for codons 500 and 496 were switched. In the previous version, codon 500 was shown as 14/24 and codon 496 as 9/24, whereas this values should be reversed. This mistake is not present in the text, where the values are shown correctly.
Author information
These authors contributed equally: Eva Vanbelleghem, Tim Van Damme.
Authors and Affiliations
Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen Claes, Julie De Backer & Bert Callewaert
Department of Biomolecular Medicine, Ghent University, Ghent, Belgium
Eva Vanbelleghem, Aude Beyens, Sofie Symoens, Kathleen Claes & Bert Callewaert
Department of Cardiology, Ghent University Hospital, Ghent, Belgium
Julie De Backer
Department of Pediatric Cardiology, University Hospital Brussels, Brussels, Belgium
Ilse Meerschaut
Department of Nephrology, Ghent University Hospital, Ghent, Belgium
Floris Vanommeslaeghe & Sigurd E. Delanghe
Department of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium
Jenneke van den Ende & Tessi Beyltjens
Department of Pediatrics, Genetics Unit, MassGeneral for Children, Boston, MA, USA
Eleanor R. Scimone & Angela E. Lin
Cardiovascular Genetics Program, Cardiology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA
Mark E. Lindsay
Pediatric Cardiology Division, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA
Mark E. Lindsay
Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA
Lisa A. Schimmenti
Division of Rheumatology, Mayo Clinic, Rochester, MN, USA
Alicia M. Hinze
Department of Pediatrics, Division of Medical Genetic, Stanford University, Stanford, CA, USA
Emily Dunn & Natalia Gomez-Ospina
ULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium
Isabelle Vandernoot, Thomas Delguste & Sandra Coppens
Paris Cité University, Centre of Reference for Constitutional Bone Diseases (MOC), Department of Genetics, INSERM UMR 1163, Imagine Institute, Necker-Enfants Malades Hospital, Paris, France
Valérie Cormier-Daire
Molecular Genetics and Functional Genomics, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
Marco Tartaglia
Medical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy
Livia Garavelli
Institute for Human Genetics and Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA
Joseph Shieh
Department of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey
Şenol Demir
Department of Medical Genetics, Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey
Esra Arslan Ateş
Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany
Martin Zenker
Department of Medicine, Division of Translational Medicine & Human Genetics, University of Pennsylvania, Philadelphia, PA, USA
Mersedeh Rohanizadegan
Division of Reproductive Endocrinology and Infertility, Stanford University School of Medicine, Stanford, CA, USA
Greysha Rivera-Cruz
Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway
Sofia Douzgou
Myhre Syndrome Foundation, Richardson, TX, USA
Justin Smith, Jessica Simkins, Don Clark, Stephanie Karatsinides, Sandy Taylor, Ines White, Patti Schultz, Kate Wears, Levi Holder & Kathy Young
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- , Stephanie Karatsinides
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- , Kate Wears
- , Levi Holder
- & Kathy Young
Corresponding author
Correspondence to Bert Callewaert.
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Vanbelleghem, E., Van Damme, T., Beyens, A. et al. Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. Eur J Hum Genet (2024). https://doi.org/10.1038/s41431-024-01690-z
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DOI: https://doi.org/10.1038/s41431-024-01690-z
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