Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
Steven Laurie(Centro Nacional de Análisis Genómico), Catarina Olimpio(University of Cambridge), Tobias B. Haack(Technical University of Munich), Elisa Benetti(University of Siena), Enzo Cohen(Inserm), Adam Jackson(Sanford Health), Vincenzo Nigro(University of Campania "Luigi Vanvitelli"), Rita Horváth(University of Cambridge), Daniel Daniš(Jackson Laboratory), Holger Hengel(University Children's Hospital Tübingen), José Garcia‐Pelaez(Universidade do Porto), Mallory Freeberg(European Bioinformatics Institute), Kiran Polavarapu(University of Ottawa), Anna Marcé‐Grau(Universitat Autònoma de Barcelona), Hanns Lochmüller(University of Ottawa), Kornelia Ellwanger(University of Hohenheim), Jean‐Madeleine de Sainte Agathe(Centre National de la Recherche Scientifique), Gemma Bullich(Centro Nacional de Análisis Genómico), Jordi Díaz‐Manera(Newcastle upon Tyne Hospitals NHS Foundation Trust), Lennart Johansson(University Medical Center Groningen), Anne‐Sophie Denommé‐Pichon(Inserm), Jonathan Baets(University of Antwerp), Coline Thomas(European Bioinformatics Institute), Anna Sommer(Helmholtz Zentrum München), Francesco Muntoni(Great Ormond Street Hospital), Marcos Fernandez-Callejo(Centro Nacional de Análisis Genómico), Laurence Faivre(Université de Bourgogne), German Demidov(University of Tübingen), Léna Guillot‐Noël(Centre National de la Recherche Scientifique), Stefan Aretz(University of Bonn), Francesco Musacchia(University of Campania "Luigi Vanvitelli"), Erik-Jan Kamsteeg(Radboud University Nijmegen), Alfons Macaya(Universitat Autònoma de Barcelona)
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