Article (Scientific journals)
Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.
Reversade, Bruno; Escande-Beillard, Nathalie; Dimopoulou, Aikaterini et al.
2022In Nature Genetics, 54 (2), p. 213
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Keywords :
Genetics
Abstract :
[en] 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.”.
Disciplines :
Genetics & genetic processes
Author, co-author :
Reversade, Bruno;  Institute of Medical Biology, A*STAR, Singapore, Singapore. bruno@reversade.com
Escande-Beillard, Nathalie;  Institute of Medical Biology, A*STAR, Singapore, Singapore
Dimopoulou, Aikaterini;  Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany
Fischer, Björn;  Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany
Chng, Serene C;  Institute of Medical Biology, A*STAR, Singapore, Singapore
Li, Yun;  Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany
Shboul, Mohammad;  Institute of Medical Biology, A*STAR, Singapore, Singapore
Tham, Puay-Yoke;  Institute of Medical Biology, A*STAR, Singapore, Singapore
Kayserili, Hülya;  Medical Genetics Department, Istanbul Medical Faculty, University of Istanbul, Istanbul, Turkey
Al-Gazali, Lihadh;  Department of Paediatrics, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates
Shahwan, Monzer;  National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan
Brancati, Francesco;  Ospedale Casa Sollievo della Sofferenza (CSS), San Giovanni Rotondo and Istituto CSS-Mendel, Rome, Italy ; Centro Studi Invecchiamento (Ce.S.I.), Department of Biomedical Sciences, Gabriele d'Annunzio University, Chieti, Italy
Lee, Hane;  Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA
O'Connor, Brian D;  Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA
Kegler, Mareen Schmidt-von;  Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany ; Max Planck Institute for Molecular Genetics, Berlin, Germany
Merriman, Barry;  Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA
Nelson, Stanley F;  Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA
Masri, Amira;  Departments of Pediatrics, Obstetrics and Gynecology, Faculty of Medicine, The University of Jordan, Amman, Jordan
Alkazaleh, Fawaz;  Departments of Pediatrics, Obstetrics and Gynecology, Faculty of Medicine, The University of Jordan, Amman, Jordan
Guerra, Deanna;  Department of Biomedical Sciences, University of Modena and Reggio Emilia, Modena, Italy
Ferrari, Paola;  Department of Pediatrics, University of Modena and Reggio Emilia, Modena, Italy
Nanda, Arti;  As'ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait City, Kuwait
Rajab, Anna;  Genetic Unit, Directorate General of Health Affairs, Ministry of Health, Muscat, Sultanate of Oman
Markie, David;  Department of Pathology, University of Otago, Dunedin, New Zealand
Gray, Mary;  Department of Pathology, University of Otago, Dunedin, New Zealand
Nelson, John;  Genetic Services of Western Australia, King Edward Memorial Hospital for Women, Perth, Australia
Grix, Arthur;  The Permanente Medical Group, Sacramento, California, USA
Sommer, Annemarie;  The Ohio State University College of Medicine and Nationwide Children's Hospital, Molecular and Human Genetics, Columbus, Ohio, USA
Savarirayan, Ravi;  University of Melbourne, Murdoch Childrens Research Institute, Royal Children's Hospital, and Genetic Health Services Victoria, Parkville, Victoria, Australia
Janecke, Andreas R;  Division of Clinical Genetics, Innsbruck Medical University, Innsbruck, Austria
Steichen, Elisabeth;  Klinik fuer Kinder- und Jugendheilkunde, Universitaet Innsbruck, Innsbruck, Austria
Sillence, David;  Department of Clinical Genetics, The Children's Hospital at Westmead, Sydney, New South Wales, Australia
Haußer, Ingrid;  Universitaets-Hautklinik Heidelberg, Heidelberg, Germany
Budde, Birgit;  Cologne Center for Genomics, Universität zu, Köln, Germany
Nürnberg, Gudrun;  Cologne Center for Genomics, Universität zu, Köln, Germany
Nürnberg, Peter;  Cologne Center for Genomics, Universität zu, Köln, Germany
Seemann, Petra;  Max Planck Institute for Molecular Genetics, Berlin, Germany ; Berlin-Brandenburg Center for Regenerative Therapies, Charité Universitaetsmedizin, Berlin, Germany
Kunkel, Désirée;  Berlin-Brandenburg Center for Regenerative Therapies, Charité Universitaetsmedizin, Berlin, Germany
Zambruno, Giovanna;  Laboratory of Molecular and Cell Biology, Istituto Dermopatico dell'Immacolata-Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy
Dallapiccola, Bruno;  Ospedale Casa Sollievo della Sofferenza (CSS), San Giovanni Rotondo and Istituto CSS-Mendel, Rome, Italy
Schuelke, Markus;  Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité Universitaetsmedizin, Berlin, Germany
Robertson, Stephen;  Department of Paediatrics and Child Health, University of Otago, Dunedin, New Zealand
Hamamy, Hanan;  National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan
Wollnik, Bernd;  Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany ; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany ; Institute of Human Genetics, University of Cologne, Cologne, Germany
Van Maldergem, Lionel ;  Centre de Génétique Humaine, Centre Hospitalier Universitaire du Sart-Tilman, Université de Lié ge, Lié ge, Belgium
Mundlos, Stefan;  Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany. stefan.mundlos@charite.de ; Max Planck Institute for Molecular Genetics, Berlin, Germany. stefan.mundlos@charite.de ; Berlin-Brandenburg Center for Regenerative Therapies, Charité Universitaetsmedizin, Berlin, Germany. stefan.mundlos@charite.de
Kornak, Uwe;  Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany ; Max Planck Institute for Molecular Genetics, Berlin, Germany
More authors (37 more) Less
Language :
English
Title :
Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.
Alternative titles :
[en] Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features (Nature Genetics, (2009), 41, 9, (1016-1021), 10.1038/ng.413)
Publication date :
February 2022
Journal title :
Nature Genetics
ISSN :
1061-4036
eISSN :
1546-1718
Publisher :
Springer Science and Business Media LLC, United States
Volume :
54
Issue :
2
Pages :
213
Peer reviewed :
Peer Reviewed verified by ORBi
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