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Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.
Zurek, Birte; Ellwanger, Kornelia; Vissers, Lisenka E L M; Schüle, Rebecca; Synofzik, Matthis; Töpf, Ana; de Voer, Richarda M; Laurie, Steven; Matalonga, Leslie; Gilissen, Christian; Ossowski, Stephan; 't Hoen, Peter A C; Vitobello, Antonio; Schulze-Hentrich, Julia M; Riess, Olaf; Brunner, Han G; Brookes, Anthony J; Rath, Ana; Bonne, Gisèle; Gumus, Gulcin; Verloes, Alain; Hoogerbrugge, Nicoline; Evangelista, Teresinha; Harmuth, Tina; Swertz, Morris; Spalding, Dylan; Hoischen, Alexander; Beltran, Sergi; Graessner, Holm.
Afiliação
  • Zurek B; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Ellwanger K; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Vissers LELM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Schüle R; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Synofzik M; Department of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.
  • Töpf A; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • de Voer RM; Department of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.
  • Laurie S; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Matalonga L; John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Gilissen C; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Ossowski S; Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
  • 't Hoen PAC; CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Vitobello A; CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Schulze-Hentrich JM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Riess O; Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
  • Brunner HG; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Brookes AJ; Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
  • Rath A; Center for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Bonne G; Inserm-University of Burgundy-Franche Comté, Dijon, France.
  • Gumus G; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Verloes A; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Hoogerbrugge N; Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
  • Evangelista T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Harmuth T; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Swertz M; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Spalding D; Department of Genetics and Genome Biology, University of Leicester, Leicester, UK.
  • Hoischen A; INSERM, US14-Orphanet, Plateforme Maladies Rares, Paris, France.
  • Beltran S; Sorbonne Université, INSERM UMRS 974, Center of Research in Myology, Paris, France.
  • Graessner H; EURORDIS-Rare Diseases Europe, Barcelona, Spain.
Eur J Hum Genet ; 29(9): 1459-1461, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34385672
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha