Solving unsolved rare neurological diseases—a Solve-RD viewpoint
Marc Sturm(University of Tübingen), Giovanni Stévanin(Inserm), Alfons Macaya(Universitat Autònoma de Barcelona), Jennifer Reichbauer(German Center for Neurodegenerative Diseases), Tobias B. Haack(Technical University of Munich), Patrick F. Chinnery(Wellcome Centre for Mitochondrial Research), Nienke van Os(Radboud University Nijmegen), Matthis Synofzik(German Center for Neurodegenerative Diseases), Rita Horváth(University of Cambridge), Corrie E. Erasmus(Radboud University Medical Center), Alexander Münchau(University of Lübeck), Anna Marcé‐Grau(Universitat Autònoma de Barcelona), Dagmar Timmann(University of Duisburg-Essen), Christoph Kamsteeg(Radboud University Nijmegen), Kornelia Ellwanger(University of Hohenheim), Carlo Wilke(German Center for Neurodegenerative Diseases), Jonathan Baets(University of Antwerp), Holm Graeßner(University Children's Hospital Tübingen), Henry Houlden(Queen Mary University of London), Steven Laurie(Centre for Genomic Regulation), Birte Zurek(University of Cologne), Alexandra Dürr(Centre National de la Recherche Scientifique), Judit Molnar(Semmelweis University), Andrea Bevot(University Children's Hospital Tübingen), Stephan Ossowski(University of Tübingen), Melanie Wayand(German Center for Neurodegenerative Diseases), Holger Hengel(German Center for Neurodegenerative Diseases), German Demidov(University of Tübingen), Erik-Jan Kamsteeg(Radboud University Nijmegen), Stephan Züchner(University of Miami), Péter Balicza(Semmelweis University), Olaf Rieß(University of Tübingen), Vincent Timmerman(University of Antwerp), Borut Peterlin(University of Ljubljana)
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