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Zurek B, Ellwanger K, Vissers LELM, et al. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. Eur J Hum Genet. 2021;29(9):1459-1461doi: 10.1038/s41431-021-00936-4.
Zurek, B., Ellwanger, K., Vissers, L. E. L. M., Schüle, R., Synofzik, M., Töpf, A., de Voer, R. M., Laurie, S., Matalonga, L., Gilissen, C., Ossowski, S., 't Hoen, P. A. C., Vitobello, A., Schulze-Hentrich, J. M., Riess, O., Brunner, H. G., Brookes, A. J., Rath, A., Bonne, G., Gumus, G., Verloes, A., Hoogerbrugge, N., Evangelista, T., Harmuth, T., Swertz, M., Spalding, D., Hoischen, A., Beltran, S., Graessner, H. (2021). Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. European journal of human genetics : EJHG, 29(9), 1459-1461. https://doi.org/10.1038/s41431-021-00936-4
Zurek, Birte, et al. "Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases." European journal of human genetics : EJHG vol. 29,9 (2021): 1459-1461. doi: https://doi.org/10.1038/s41431-021-00936-4
Zurek B, Ellwanger K, Vissers LELM, Schüle R, Synofzik M, Töpf A, de Voer RM, Laurie S, Matalonga L, Gilissen C, Ossowski S, 't Hoen PAC, Vitobello A, Schulze-Hentrich JM, Riess O, Brunner HG, Brookes AJ, Rath A, Bonne G, Gumus G, Verloes A, Hoogerbrugge N, Evangelista T, Harmuth T, Swertz M, Spalding D, Hoischen A, Beltran S, Graessner H. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. Eur J Hum Genet. 2021 Sep;29(9):1459-1461. doi: 10.1038/s41431-021-00936-4. PMID: 34385672; PMCID: PMC8440583.
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Eur J Hum Genet. 2021 Sep;29(9):1459-1461. doi: 10.1038/s41431-021-00936-4.

Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.

European journal of human genetics : EJHG

Birte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Richarda M de Voer, Steven Laurie, Leslie Matalonga, Christian Gilissen, Stephan Ossowski, Peter A C 't Hoen, Antonio Vitobello, Julia M Schulze-Hentrich, Olaf Riess, Han G Brunner, Anthony J Brookes, Ana Rath, Gisèle Bonne, Gulcin Gumus, Alain Verloes, Nicoline Hoogerbrugge, Teresinha Evangelista, Tina Harmuth, Morris Swertz, Dylan Spalding, Alexander Hoischen, Sergi Beltran, Holm Graessner,

Affiliations

  1. Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  2. Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  3. Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  4. Department of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.
  5. German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  6. John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  7. Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
  8. CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
  9. Center for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, The Netherlands.
  10. Inserm-University of Burgundy-Franche Comté, Dijon, France.
  11. Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
  12. Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
  13. Department of Genetics and Genome Biology, University of Leicester, Leicester, UK.
  14. INSERM, US14-Orphanet, Plateforme Maladies Rares, Paris, France.
  15. Sorbonne Université, INSERM UMRS 974, Center of Research in Myology, Paris, France.
  16. EURORDIS-Rare Diseases Europe, Barcelona, Spain.
  17. Genetics Department, APHP-Robert Debré University Hospital, Université de Paris, Paris, France.
  18. Department of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  19. European Bioinformatics Institute, European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  20. Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, The Netherlands.
  21. Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  22. Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona (UB), Barcelona, Spain.
  23. Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. [email protected].
  24. Centre for Rare Diseases, University of Tübingen, Tübingen, Germany. [email protected].

PMID: 34385672 PMCID: PMC8440583 DOI: 10.1038/s41431-021-00936-4

[No abstract available.]

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