Correction to: Nature Genetics https://doi.org/10.1038/ng.413, published online 2 August 2009.
In the version of this article initially published, there was an omission in the Acknowledgements section for support to Hülya Kayserili. The Acknowledgements should have ended with the text “and a grant from TUBITAK SBAG-108S418 to H.K.”
Author information
These authors contributed equally: Bruno Reversade, Nathalie Escande-Beillard.
Authors and Affiliations
Institute of Medical Biology, A*STAR, Singapore, Singapore
Bruno Reversade, Nathalie Escande-Beillard, Serene C. Chng, Mohammad Shboul & Puay-Yoke Tham
Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany
Aikaterini Dimopoulou, Björn Fischer, Mareen Schmidt-von Kegler, Stefan Mundlos & Uwe Kornak
Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany
Yun Li & Bernd Wollnik
Medical Genetics Department, Istanbul Medical Faculty, University of Istanbul, Istanbul, Turkey
Hülya Kayserili
Department of Paediatrics, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates
Lihadh Al-Gazali
National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan
Monzer Shahwan & Hanan Hamamy
Ospedale Casa Sollievo della Sofferenza (CSS), San Giovanni Rotondo and Istituto CSS-Mendel, Rome, Italy
Francesco Brancati & Bruno Dallapiccola
Centro Studi Invecchiamento (Ce.S.I.), Department of Biomedical Sciences, Gabriele d’Annunzio University, Chieti, Italy
Francesco Brancati
Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA
Hane Lee, Brian D. O’Connor, Barry Merriman & Stanley F. Nelson
Max Planck Institute for Molecular Genetics, Berlin, Germany
Mareen Schmidt-von Kegler, Petra Seemann, Stefan Mundlos & Uwe Kornak
Departments of Pediatrics, Obstetrics and Gynecology, Faculty of Medicine, The University of Jordan, Amman, Jordan
Amira Masri & Fawaz Alkazaleh
Department of Biomedical Sciences, University of Modena and Reggio Emilia, Modena, Italy
Deanna Guerra
Department of Pediatrics, University of Modena and Reggio Emilia, Modena, Italy
Paola Ferrari
As’ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait City, Kuwait
Arti Nanda
Genetic Unit, Directorate General of Health Affairs, Ministry of Health, Muscat, Sultanate of Oman
Anna Rajab
Department of Pathology, University of Otago, Dunedin, New Zealand
David Markie & Mary Gray
Genetic Services of Western Australia, King Edward Memorial Hospital for Women, Perth, Australia
John Nelson
The Permanente Medical Group, Sacramento, California, USA
Arthur Grix
The Ohio State University College of Medicine and Nationwide Children’s Hospital, Molecular and Human Genetics, Columbus, Ohio, USA
Annemarie Sommer
University of Melbourne, Murdoch Childrens Research Institute, Royal Children’s Hospital, and Genetic Health Services Victoria, Parkville, Victoria, Australia
Ravi Savarirayan
Division of Clinical Genetics, Innsbruck Medical University, Innsbruck, Austria
Andreas R. Janecke
Klinik fuer Kinder- und Jugendheilkunde, Universitaet Innsbruck, Innsbruck, Austria
Elisabeth Steichen
Department of Clinical Genetics, The Children’s Hospital at Westmead, Sydney, New South Wales, Australia
David Sillence
Universitaets-Hautklinik Heidelberg, Heidelberg, Germany
Ingrid Haußer
Cologne Center for Genomics, Universität zu, Köln, Germany
Birgit Budde, Gudrun Nürnberg & Peter Nürnberg
Berlin-Brandenburg Center for Regenerative Therapies, Charité Universitaetsmedizin, Berlin, Germany
Petra Seemann, Désirée Kunkel & Stefan Mundlos
Laboratory of Molecular and Cell Biology, Istituto Dermopatico dell’Immacolata-Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy
Giovanna Zambruno
Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité Universitaetsmedizin, Berlin, Germany
Markus Schuelke
Department of Paediatrics and Child Health, University of Otago, Dunedin, New Zealand
Stephen Robertson
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany
Bernd Wollnik
Institute of Human Genetics, University of Cologne, Cologne, Germany
Bernd Wollnik
Centre de Génétique Humaine, Centre Hospitalier Universitaire du Sart-Tilman, Université de Lié ge, Lié ge, Belgium
Lionel Van Maldergem
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Correspondence to Bruno Reversade or Stefan Mundlos.
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Reversade, B., Escande-Beillard, N., Dimopoulou, A. et al. Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features. Nat Genet 54, 213 (2022). https://doi.org/10.1038/s41588-022-01013-2
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DOI: https://doi.org/10.1038/s41588-022-01013-2
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