Correction to: Nature Medicine https://doi.org/10.1038/s41591-024-03420-w, published online 17 January 2025.
In the version of this article initially published, collaborators in the Solve-RD DITF-GENTURIS, Solve-RD DITF-ITHACA, Solve-RD DITF-EURO-NMD, Solve-RD DITF-RND and Solve-RD consortia were not listed correctly as authors in the metadata associated with this paper, as is now amended in the HTML and PDF versions of the article.
Author information
These authors contributed equally: Steven Laurie, Wouter Steyaert, Elke de Boer, Kiran Polavarapu, Nika Schuermans, Anna K. Sommer.
These authors jointly supervised this work: Katja Lohmann, Richarda M. de Voer, Ana Töpf, Lisenka E. L. M. Vissers, Sergi Beltran, Alexander Hoischen.
Authors and Affiliations
Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain
Steven Laurie, Ida Paramonov, Gemma Bullich, Marcos Fernandez-Callejo, Hanns Lochmüller, Davide Piscia, Luca Zalatnai, Hanns Lochmüller, Sergi Beltran, Gemma Bullich, Marcos Fernandez-Callejo, Steven Laurie, Hanns Lochmüller, Leslie Matalonga, Ida Paramonov, Davide Piscia, Leslie Matalonga & Sergi Beltran
Universitat de Barcelona (UB), Barcelona, Spain
Steven Laurie, Ida Paramonov, Gemma Bullich, Marcos Fernandez-Callejo, Davide Piscia, Luca Zalatnai, Gemma Bullich, Marcos Fernandez-Callejo, Steven Laurie, Leslie Matalonga, Ida Paramonov, Davide Piscia & Leslie Matalonga
Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands
Wouter Steyaert, Elke de Boer, Erik-Jan Kamsteeg, Tjitske Kleefstra, Rolph Pfundt, Karolis Šablauskas, Iris B. A. W. te Paske, Jeroen van Reeuwijk, Janet Vos, Robin Wijngaard, Burcu Yaldiz, Richarda M. de Voer, Nicoline Hoogerbrugge, Iris B. A. W. te Paske, Elke de Boer, Tjitske Kleefstra, Lisenka E.L.M. Vissers, Erik-Jan Kamsteeg, Nicoline Hoogerbrugge, Christian Gilissen, Han G. Brunner, Christian Gilissen, Alexander Hoischen, Nicoline Hoogerbrugge, Erik-Jan Kamsteeg, Tjitske Kleefstra, Karolis Šablauskas, Wouter Steyaert, Nicoline Hoogerbrugge, Burcu Yaldiz, Christian Gilissen, Nicoline Hoogerbrugge, Han G. Brunner, Richarda M. de Voer, Lisenka E.L.M. Vissers & Alexander Hoischen
Radboud Institute for Medical Innovation, Nijmegen, the Netherlands
Wouter Steyaert, Iris B. A. W. te Paske, Janet Vos, Robin Wijngaard, Richarda M. de Voer, Nicoline Hoogerbrugge, Iris B. A. W. te Paske, Nicoline Hoogerbrugge, Christian Gilissen, Christian Gilissen, Alexander Hoischen, Nicoline Hoogerbrugge, Wouter Steyaert, Nicoline Hoogerbrugge, Christian Gilissen, Nicoline Hoogerbrugge, Richarda M. de Voer & Alexander Hoischen
Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands
Elke de Boer, Tjitske Kleefstra, Rolph Pfundt, Bart van de Warrenburg, Jeroen van Reeuwijk, Elke de Boer, Tjitske Kleefstra, Lisenka E.L.M. Vissers, Bart van de Warrenburg, Han G. Brunner, Tjitske Kleefstra, Han G. Brunner & Lisenka E.L.M. Vissers
Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada
Kiran Polavarapu, Hanns Lochmüller, Rachel Thompson, Hanns Lochmüller, Kiran Polavarapu, Rachel Thompson, Hanns Lochmüller, Kiran Polavarapu & Rachel Thompson
Program for Undiagnosed Rare Diseases (UD-PrOZA), Ghent University Hospital, Ghent, Belgium
Nika Schuermans, Nika Schuermans & Nika Schuermans
Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium
Nika Schuermans, Nika Schuermans & Nika Schuermans
Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium
Nika Schuermans, Nika Schuermans & Nika Schuermans
Institute of Human Genetics, Medical Faculty, University of Bonn, Bonn, Germany
Anna K. Sommer, Stefan Aretz, Sophia Peters, Stefan Aretz, Sophia Peters, Anna K. Sommer, Stefan Aretz, Sophia Peters & Anna K. Sommer
Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany
German Demidov, Kornelia Ellwanger, Tobias B. Haack, Leon Schütz, Marc Sturm, Jishu Xu, Birte Zurek, Tobias B. Haack, Olaf Riess, Holm Graessner, Tobias B. Haack, Olaf Riess, Jishu Xu, Holm Graessner, German Demidov, Kornelia Ellwanger, Holm Graessner, Tobias B. Haack, Stephan Ossowski, Olaf Riess, Marc Sturm, Stephan Ossowski, Jishu Xu, Birte Zurek, Holm Graessner, Stephan Ossowski & Olaf Riess
European Bioinformatics Institute, European Molecular Biology Laboratory, Cambridge, UK
Coline Thomas, Mallory Freeberg, Mallory Freeberg & Coline Thomas
Center for Hereditary Tumor Syndromes, University Hospital Bonn, Bonn, Germany
Stefan Aretz, Stefan Aretz & Stefan Aretz
Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
Jonathan Baets, Liedewei Van de Vondel, Jonathan Baets, Liedewei Van de Vondel, Jonathan Baets & Jonathan Baets
Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium
Jonathan Baets, Liedewei Van de Vondel, Jonathan Baets, Liedewei Van de Vondel, Jonathan Baets & Jonathan Baets
Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Antwerp, Belgium
Jonathan Baets, Jonathan Baets, Jonathan Baets & Jonathan Baets
Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy
Elisa Benetti, Alessandra Renieri, Alessandra Renieri, Elisa Benetti & Alessandra Renieri
Medical Genetics, University of Siena, Siena, Italy
Elisa Benetti, Alessandra Renieri, Alessandra Renieri, Elisa Benetti & Alessandra Renieri
Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK
Patrick F. Chinnery, Rita Horvath, Catarina Olimpio, Patrick F. Chinnery, Rita Horvath, Catarina Olimpio, Patrick F. Chinnery, Rita Horvath, Patrick F. Chinnery & Rita Horvath
Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge, UK
Patrick F. Chinnery, Patrick F. Chinnery, Patrick F. Chinnery & Patrick F. Chinnery
Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK
Jill Clayton-Smith, Adam Jackson, Jill Clayton-Smith, Adam Jackson, Jill Clayton-Smith & Adam Jackson
Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester University Hospitals NHS Foundation Trust, Health Innovation Manchester, Manchester, UK
Jill Clayton-Smith, Adam Jackson, Jill Clayton-Smith, Adam Jackson, Jill Clayton-Smith & Adam Jackson
Centre de Recherche en Myologie, Sorbonne Université, Inserm, Institut de Myologie, Paris, France
Enzo Cohen, Isabelle Nelson, Enzo Cohen, Teresinha Evangelista, Isabelle Nelson, Enzo Cohen, Teresinha Evangelista, Isabelle Nelson, Teresinha Evangelista & Teresinha Evangelista
Jackson Laboratory for Genomic Medicine, Farmington, CT, USA
Daniel Danis & Daniel Danis
Department of Genetics, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, Pitié-Salpêtrière University Hospital, Paris, France
Jean-Madeleine de Sainte Agathe & Jean-Madeleine de Sainte Agathe
University of Burgundy, Dijon, France
Anne-Sophie Denommé-Pichon, Laurence Faivre, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Laurence Faivre, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Laurence Faivre & Antonio Vitobello
Functional Unit for Diagnostic Innovation in Rare Diseases, Dijon Bourgogne University Hospital, Dijon, France
Anne-Sophie Denommé-Pichon, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Antonio Vitobello, Anne-Sophie Denommé-Pichon & Antonio Vitobello
John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK
Jordi Diaz-Manera, Volker Straub, Christina Trainor, Ana Töpf, Jordi Diaz-Manera, Volker Straub, Ana Töpf, Ana Töpf & Ana Töpf
Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK
Stephanie Efthymiou, Henry Houlden, Heba Morsy, Jana Vandrovcova, Henry Houlden, Jana Vandrovcova, Stephanie Efthymiou, Henry Houlden, Heba Morsy, Jana Vandrovcova, Stephanie Efthymiou, Henry Houlden, Heba Morsy & Jana Vandrovcova
Genetics Department, Dijon University Hospital, Dijon, France
Laurence Faivre, Laurence Faivre & Laurence Faivre
Centre of Reference for Rare Diseases: Development Disorders and Malformation Syndromes, Dijon University Hospital, Dijon, France
Laurence Faivre, Laurence Faivre & Laurence Faivre
University of Burgundy-Franche Comté, Dijon, France
Laurence Faivre, Laurence Faivre & Laurence Faivre
GIMI institute, Dijon University Hospital, Dijon, France
Laurence Faivre, Laurence Faivre & Laurence Faivre
Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal
José Garcia-Pelaez, José Garcia-Pelaez & José Garcia-Pelaez
IPATIMUP – Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal
José Garcia-Pelaez, Carla Oliveira, José Garcia-Pelaez, Carla Oliveira, José Garcia-Pelaez & Carla Oliveira
Faculty of Medicine, University of Porto, Porto, Portugal
José Garcia-Pelaez, Carla Oliveira, José Garcia-Pelaez, Carla Oliveira, José Garcia-Pelaez & Carla Oliveira
Institut du Cerveau, Sorbonne University, Paris, France
Lena Guillot-Noel, Carla Oliveira, Giovanni Stevanin, Carla Oliveira, Lena Guillot-Noel, Giovanni Stevanin, Lena Guillot-Noel, Carla Oliveira & Giovanni Stevanin
MRC Centre for Neuromuscular Diseases and National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, London, UK
Mike Hanna, Mike Hanna & Mike Hanna
Department of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany
Holger Hengel, Melanie Kellner, Selina Reich, Ludger Schöls, Carlo Wilke, Jishu Xu, Holger Hengel, Melanie Kellner, Selina Reich, Ludger Schöls, Rebecca Schüle, Matthis Synofzik, Carlo Wilke, Jishu Xu, Holger Hengel, Melanie Kellner, Ludger Schöls, Rebecca Schüle, Matthis Synofzik, Carlo Wilke, Jishu Xu, Rebecca Schüle & Matthis Synofzik
German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany
Holger Hengel, Melanie Kellner, Selina Reich, Ludger Schöls, Carlo Wilke, Jishu Xu, Holger Hengel, Melanie Kellner, Selina Reich, Ludger Schöls, Rebecca Schüle, Matthis Synofzik, Carlo Wilke, Jishu Xu, Holger Hengel, Melanie Kellner, Ludger Schöls, Rebecca Schüle, Matthis Synofzik, Carlo Wilke, Jishu Xu, Rebecca Schüle & Matthis Synofzik
Department of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
Lennart Johansson, Morris A. Swertz, Lennart Johansson & Morris A. Swertz
Folkhälsan Research Centre and Medicum, University of Helsinki, Helsinki, Finland
Mridul Johari, Marco Savarese, Bjarne Udd, Mridul Johari, Marco Savarese, Bjarne Udd, Mridul Johari, Marco Savarese & Bjarne Udd
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Tjitske Kleefstra, Tjitske Kleefstra & Tjitske Kleefstra
Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, the Netherlands
Tjitske Kleefstra, Tjitske Kleefstra & Tjitske Kleefstra
MRGM, Maladies Rares: Génétique et Métabolisme, INSERM U1211, Université de Bordeaux, Bordeaux, France
Didier Lacombe, Didier Lacombe & Didier Lacombe
Service de Génétique Médicale, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France
Didier Lacombe, Didier Lacombe & Didier Lacombe
Department of Neuropediatrics and Muscle Disorders, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Hanns Lochmüller, Hanns Lochmüller & Hanns Lochmüller
Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada
Hanns Lochmüller, Hanns Lochmüller & Hanns Lochmüller
Brain and Mind Research Institute, University of Ottawa, Ottawa, Ontario, Canada
Hanns Lochmüller, Hanns Lochmüller & Hanns Lochmüller
Institute of Rare Diseases Research, Spanish Undiagnosed Rare Diseases Cases Program (SpainUDP) & Undiagnosed Diseases Network International (UDNI), Instituto de Salud Carlos III, Madrid, Spain
Estrella López-Martín, Manuel Posada, Estrella López-Martín, Manuel Posada, Estrella López-Martín & Manuel Posada
Pediatric Neurology Research Group, Vall d’Hebron Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain
Alfons Macaya, Anna Marcé-Grau, Alfons Macaya, Anna Marcé-Grau, Alfons Macaya & Anna Marcé-Grau
Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia
Aleš Maver, Borut Peterlin, Aleš Maver, Borut Peterlin, Aleš Maver & Borut Peterlin
Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt
Heba Morsy, Heba Morsy & Heba Morsy
Dubowitz Neuromuscular Centre, UCL Great Ormond Street Hospital, London, UK
Francesco Muntoni, Francesco Muntoni & Francesco Muntoni
NIHR Great Ormond Street Hospital Biomedical Research Centre, London, UK
Francesco Muntoni, Francesco Muntoni & Francesco Muntoni
Dipartimento di Medicina di Precisione, Università degli Studi della Campania “Luigi Vanvitelli”, Naples, Italy
Francesco Musacchia, Vincenzo Nigro, Giulio Piluso, Annalaura Torella, Vincenzo Nigro, Annalaura Torella, Francesco Musacchia, Vincenzo Nigro, Giulio Piluso, Annalaura Torella, Francesco Musacchia, Vincenzo Nigro, Giulio Piluso & Annalaura Torella
Telethon Institute of Genetics and Medicine, Pozzuoli, Italy
Francesco Musacchia, Vincenzo Nigro, Annalaura Torella, Vincenzo Nigro, Annalaura Torella, Francesco Musacchia, Vincenzo Nigro, Annalaura Torella, Francesco Musacchia, Vincenzo Nigro & Annalaura Torella
East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK
Catarina Olimpio & Catarina Olimpio
Centre of Hereditary Ataxia, Department of Neurology, Charles University Prague–2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic
Jaroslava Paulasová Schwabová
Institute of Systems Motor Science, University of Lübeck, Lübeck, Germany
Martje G. Pauly, Martje G. Pauly & Martje G. Pauly
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
Martje G. Pauly, Katja Lohmann, Martje G. Pauly, Katja Lohmann, Martje G. Pauly & Katja Lohmann
Department of Neurology, University Hospital Schleswig Holstein, Lübeck, Germany
Martje G. Pauly, Martje G. Pauly & Martje G. Pauly
Genetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy
Alessandra Renieri, Alessandra Renieri & Alessandra Renieri
Department of Biology and Medical Genetics, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic
Lukas Ryba, Emílie Vyhnálková & Lukas Ryba
Institute of Data Science and Digital Technologies, Vilnius University, Vilnius, Lithuania
Karolis Šablauskas & Karolis Šablauskas
Medizinische Klinik und Poliklinik IV – Campus Innenstadt, Klinikum der Universität München, Munich, Germany
Verena Steinke-Lange, Verena Steinke-Lange & Verena Steinke-Lange
MGZ – Medical Genetics Center, Munich, Germany
Verena Steinke-Lange, Verena Steinke-Lange & Verena Steinke-Lange
Molecular Genetics and Functional Genomics, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy
Marco Tartaglia & Marco Tartaglia
Tampere Neuromuscular Center, Tampere, Finland
Bjarne Udd, Bjarne Udd & Bjarne Udd
Vasa Central Hospital, Vaasa, Finland
Bjarne Udd, Bjarne Udd & Bjarne Udd
Peripheral Neuropathy Research Group, University of Antwerp, Antwerp, Belgium
Liedewei Van de Vondel & Liedewei Van de Vondel
Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands
Bart van de Warrenburg & Bart van de Warrenburg
Institute of Clinical Genetics, University Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany
Doreen William & Doreen William
National Center for Tumor Diseases (NCT), Dresden, Germany
Doreen William & Doreen William
Department of Genetics and Genome Biology, University of Leicester, Leicester, UK
Anthony J. Brookes, Anthony J. Brookes & Anthony J. Brookes
Centre for Rare Diseases, University of Tübingen, Tübingen, Germany
Olaf Riess, Holm Graessner, Olaf Riess, Holm Graessner, Holm Graessner, Olaf Riess, Holm Graessner & Olaf Riess
NGS Competence Center Tübingen (NCCT), University of Tübingen, Tübingen, Germany
Stephan Ossowski, Stephan Ossowski & Stephan Ossowski
Dept of Genetics, Assistance Publique-Hôpitaux de Paris, Université de Paris, Robert DEBRE University Hospital, Paris, France
Alain Verloes, Alain Verloes & Alain Verloes
INSERM UMR 1141 “NeuroDiderot”, Hôpital Robert DEBRE, Paris, France
Alain Verloes, Alain Verloes & Alain Verloes
Department of Clinical Genetics, Maastricht University Medical Centre and GROW School for Development and Oncology, University of Maastricht, Maastricht, the Netherlands
Han G. Brunner & Han G. Brunner
Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona (UB), Barcelona, Spain
Sergi Beltran & Sergi Beltran
Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands
Alexander Hoischen & Alexander Hoischen
- Steven Laurie
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Consortia
Solve-RD DITF-GENTURIS
- Stefan Aretz
- , Richarda M. de Voer
- , José Garcia-Pelaez
- , Nicoline Hoogerbrugge
- , Carla Oliveira
- , Sophia Peters
- , Anna K. Sommer
- , Verena Steinke-Lange
- , Iris B. A. W. te Paske
- & Doreen William
Solve-RD DITF-ITHACA
- Elke de Boer
- , Jill Clayton-Smith
- , Jean-Madeleine de Sainte Agathe
- , Anne-Sophie Denommé-Pichon
- , Laurence Faivre
- , Tobias B. Haack
- , Adam Jackson
- , Tjitske Kleefstra
- , Didier Lacombe
- , Estrella López-Martín
- , Vincenzo Nigro
- , Manuel Posada
- , Alessandra Renieri
- , Olaf Riess
- , Lukas Ryba
- , Annalaura Torella
- , Alain Verloes
- , Lisenka E.L.M. Vissers
- & Antonio Vitobello
Solve-RD DITF-EURO-NMD
- Jonathan Baets
- , Patrick F. Chinnery
- , Enzo Cohen
- , Teresinha Evangelista
- , Rita Horvath
- , Henry Houlden
- , Mridul Johari
- , Hanns Lochmüller
- , Francesco Muntoni
- , Francesco Musacchia
- , Isabelle Nelson
- , Vincenzo Nigro
- , Catarina Olimpio
- , Giulio Piluso
- , Kiran Polavarapu
- , Marco Savarese
- , Rachel Thompson
- , Ana Töpf
- , Annalaura Torella
- , Bjarne Udd
- , Liedewei Van de Vondel
- & Jana Vandrovcova
Solve-RD DITF-RND
- Jonathan Baets
- , Patrick F. Chinnery
- , Stephanie Efthymiou
- , Holm Graessner
- , Lena Guillot-Noel
- , Tobias B. Haack
- , Mike Hanna
- , Holger Hengel
- , Rita Horvath
- , Henry Houlden
- , Erik-Jan Kamsteeg
- , Melanie Kellner
- , Katja Lohmann
- , Alfons Macaya
- , Anna Marcé-Grau
- , Aleš Maver
- , Heba Morsy
- , Martje G. Pauly
- , Borut Peterlin
- , Selina Reich
- , Olaf Riess
- , Ludger Schöls
- , Rebecca Schüle
- , Nika Schuermans
- , Giovanni Stevanin
- , Matthis Synofzik
- , Nicoline Hoogerbrugge
- , Bart van de Warrenburg
- , Jana Vandrovcova
- , Carlo Wilke
- & Jishu Xu
Solve-RD consortium
- Stefan Aretz
- , Jonathan Baets
- , Sergi Beltran
- , Elisa Benetti
- , Christian Gilissen
- , Anthony J. Brookes
- , Han G. Brunner
- , Gemma Bullich
- , Patrick F. Chinnery
- , Jill Clayton-Smith
- , Enzo Cohen
- , Daniel Danis
- , Holm Graessner
- , German Demidov
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- , Jordi Diaz-Manera
- , Stephanie Efthymiou
- , Kornelia Ellwanger
- , Teresinha Evangelista
- , Laurence Faivre
- , Marcos Fernandez-Callejo
- , Mallory Freeberg
- , José Garcia-Pelaez
- , Christian Gilissen
- , Holm Graessner
- , Lena Guillot-Noel
- , Tobias B. Haack
- , Mike Hanna
- , Holger Hengel
- , Alexander Hoischen
- , Nicoline Hoogerbrugge
- , Rita Horvath
- , Henry Houlden
- , Adam Jackson
- , Lennart Johansson
- , Mridul Johari
- , Erik-Jan Kamsteeg
- , Melanie Kellner
- , Tjitske Kleefstra
- , Didier Lacombe
- , Steven Laurie
- , Hanns Lochmüller
- , Katja Lohmann
- , Estrella López-Martín
- , Alfons Macaya
- , Anna Marcé-Grau
- , Leslie Matalonga
- , Aleš Maver
- , Heba Morsy
- , Francesco Muntoni
- , Francesco Musacchia
- , Isabelle Nelson
- , Vincenzo Nigro
- , Carla Oliveira
- , Stephan Ossowski
- , Ida Paramonov
- , Martje G. Pauly
- , Borut Peterlin
- , Sophia Peters
- , Giulio Piluso
- , Davide Piscia
- , Kiran Polavarapu
- , Manuel Posada
- , Alessandra Renieri
- , Olaf Riess
- , Karolis Šablauskas
- , Marco Savarese
- , Ludger Schöls
- , Rebecca Schüle
- , Nika Schuermans
- , Anna K. Sommer
- , Verena Steinke-Lange
- , Giovanni Stevanin
- , Wouter Steyaert
- , Volker Straub
- , Marc Sturm
- , Morris A. Swertz
- , Matthis Synofzik
- , Marco Tartaglia
- , Teresinha Evangelista
- , Coline Thomas
- , Rachel Thompson
- , Ana Töpf
- , Annalaura Torella
- , Bjarne Udd
- , Nicoline Hoogerbrugge
- , Stephan Ossowski
- , Jana Vandrovcova
- , Alain Verloes
- , Ana Töpf
- , Antonio Vitobello
- , Anthony J. Brookes
- , Carlo Wilke
- , Jishu Xu
- , Burcu Yaldiz
- & Birte Zurek
Corresponding authors
Correspondence to Sergi Beltran or Alexander Hoischen.
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Laurie, S., Steyaert, W., de Boer, E. et al. Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses. Nat Med 31, 2819–2820 (2025). https://doi.org/10.1038/s41591-025-03754-z
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DOI: https://doi.org/10.1038/s41591-025-03754-z
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