Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint
Rebecca Schüle(Heidelberg University), Marc Sturm(University of Tübingen), Katja Lohmann(University of Lübeck), 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), Aleš Maver(Ljubljana University Medical Centre), 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), Leslie Matalonga(Centre for Genomic Regulation), Jana Vandrovcová(Texas Tech University), Anna Marcé‐Grau(Universitat Autònoma de Barcelona), Dagmar Timmann(University of Duisburg-Essen), Christoph Kamsteeg(Radboud University Nijmegen), Sergi Beltrán(Centro Nacional de Análisis Genómico), Kornelia Ellwanger(University of Hohenheim), Carlo Wilke(German Center for Neurodegenerative Diseases), Lüdger Schöls(German Center for Neurodegenerative Diseases), Jonathan Baets(University of Antwerp), Holm Graeßner(University Children's Hospital Tübingen), 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), Bart van de Warrenburg(Radboud University Nijmegen), 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), Giovanni Stévanin(Inserm)
Cited by 0
Related Papers
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
|Nature Genetics|2004|1.6k
Mitochondrial diseases
|Nature Reviews Disease Primers|2016|1.5k
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis
|The Lancet Neurology|2004|1.1k
Ensembl 2012
|Nucleic Acids Research|2011|839