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Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.
Reversade, Bruno; Escande-Beillard, Nathalie; Dimopoulou, Aikaterini; Fischer, Björn; Chng, Serene C; Li, Yun; Shboul, Mohammad; Tham, Puay-Yoke; Kayserili, Hülya; Al-Gazali, Lihadh; Shahwan, Monzer; Brancati, Francesco; Lee, Hane; O'Connor, Brian D; Kegler, Mareen Schmidt-von; Merriman, Barry; Nelson, Stanley F; Masri, Amira; Alkazaleh, Fawaz; Guerra, Deanna; Ferrari, Paola; Nanda, Arti; Rajab, Anna; Markie, David; Gray, Mary; Nelson, John; Grix, Arthur; Sommer, Annemarie; Savarirayan, Ravi; Janecke, Andreas R; Steichen, Elisabeth; Sillence, David; Haußer, Ingrid; Budde, Birgit; Nürnberg, Gudrun; Nürnberg, Peter; Seemann, Petra; Kunkel, Désirée; Zambruno, Giovanna; Dallapiccola, Bruno; Schuelke, Markus; Robertson, Stephen; Hamamy, Hanan; Wollnik, Bernd; Van Maldergem, Lionel; Mundlos, Stefan; Kornak, Uwe.
Afiliación
  • Reversade B; Institute of Medical Biology, A*STAR, Singapore, Singapore. bruno@reversade.com.
  • Escande-Beillard N; Institute of Medical Biology, A*STAR, Singapore, Singapore.
  • Dimopoulou A; Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany.
  • Fischer B; Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany.
  • Chng SC; Institute of Medical Biology, A*STAR, Singapore, Singapore.
  • Li Y; Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
  • Shboul M; Institute of Medical Biology, A*STAR, Singapore, Singapore.
  • Tham PY; Institute of Medical Biology, A*STAR, Singapore, Singapore.
  • Kayserili H; Medical Genetics Department, Istanbul Medical Faculty, University of Istanbul, Istanbul, Turkey.
  • Al-Gazali L; Department of Paediatrics, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
  • Shahwan M; National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan.
  • Brancati F; Ospedale Casa Sollievo della Sofferenza (CSS), San Giovanni Rotondo and Istituto CSS-Mendel, Rome, Italy.
  • Lee H; Centro Studi Invecchiamento (Ce.S.I.), Department of Biomedical Sciences, Gabriele d'Annunzio University, Chieti, Italy.
  • O'Connor BD; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.
  • Kegler MS; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.
  • Merriman B; Institute of Medical Genetics, Charité Universitaetsmedizin, Berlin, Germany.
  • Nelson SF; Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Masri A; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.
  • Alkazaleh F; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.
  • Guerra D; Departments of Pediatrics, Obstetrics and Gynecology, Faculty of Medicine, The University of Jordan, Amman, Jordan.
  • Ferrari P; Departments of Pediatrics, Obstetrics and Gynecology, Faculty of Medicine, The University of Jordan, Amman, Jordan.
  • Nanda A; Department of Biomedical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Rajab A; Department of Pediatrics, University of Modena and Reggio Emilia, Modena, Italy.
  • Markie D; As'ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait City, Kuwait.
  • Gray M; Genetic Unit, Directorate General of Health Affairs, Ministry of Health, Muscat, Sultanate of Oman.
  • Nelson J; Department of Pathology, University of Otago, Dunedin, New Zealand.
  • Grix A; Department of Pathology, University of Otago, Dunedin, New Zealand.
  • Sommer A; Genetic Services of Western Australia, King Edward Memorial Hospital for Women, Perth, Australia.
  • Savarirayan R; The Permanente Medical Group, Sacramento, California, USA.
  • Janecke AR; The Ohio State University College of Medicine and Nationwide Children's Hospital, Molecular and Human Genetics, Columbus, Ohio, USA.
  • Steichen E; University of Melbourne, Murdoch Childrens Research Institute, Royal Children's Hospital, and Genetic Health Services Victoria, Parkville, Victoria, Australia.
  • Sillence D; Division of Clinical Genetics, Innsbruck Medical University, Innsbruck, Austria.
  • Haußer I; Klinik fuer Kinder- und Jugendheilkunde, Universitaet Innsbruck, Innsbruck, Austria.
  • Budde B; Department of Clinical Genetics, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.
  • Nürnberg G; Universitaets-Hautklinik Heidelberg, Heidelberg, Germany.
  • Nürnberg P; Cologne Center for Genomics, Universität zu, Köln, Germany.
  • Seemann P; Cologne Center for Genomics, Universität zu, Köln, Germany.
  • Kunkel D; Cologne Center for Genomics, Universität zu, Köln, Germany.
  • Zambruno G; Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Dallapiccola B; Berlin-Brandenburg Center for Regenerative Therapies, Charité Universitaetsmedizin, Berlin, Germany.
  • Schuelke M; Berlin-Brandenburg Center for Regenerative Therapies, Charité Universitaetsmedizin, Berlin, Germany.
  • Robertson S; Laboratory of Molecular and Cell Biology, Istituto Dermopatico dell'Immacolata-Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy.
  • Hamamy H; Ospedale Casa Sollievo della Sofferenza (CSS), San Giovanni Rotondo and Istituto CSS-Mendel, Rome, Italy.
  • Wollnik B; Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité Universitaetsmedizin, Berlin, Germany.
  • Van Maldergem L; Department of Paediatrics and Child Health, University of Otago, Dunedin, New Zealand.
  • Mundlos S; National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan.
  • Kornak U; Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
Nat Genet ; 54(2): 213, 2022 Feb.
Article en En | MEDLINE | ID: mdl-35064218
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Singapur
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Singapur