Neurologic Phenotypes Associated With Mutations in <i>RTN4IP1</i> (<i>OPA10</i>) in Children and Young Adults
Majida Charif(Université d'Angers), Guy Lenaers(Centre National de la Recherche Scientifique), Sabine Derrien, Anna Ardissone(Fondazione IRCCS Istituto Neurologico Carlo Besta), Charu Deshpande(Guy's Hospital), Vincent Procaccio(Centre National de la Recherche Scientifique), Hamind Galehdari, Kyle Thompson(Wellcome Centre for Mitochondrial Research), Pascal Reynier(Centre National de la Recherche Scientifique), Alessia Nasca(Fondazione IRCCS Istituto Neurologico Carlo Besta), Inês A. Barbosa(King's College London), Yaumara Perdomo Trujillo, Michael A. Simpson(King's College London), David Goudenège(Inserm), Corinna Siegel(Technical University of Munich), Frances E. White(Newcastle University), Eleonora Lamantea(Istituti di Ricovero e Cura a Carattere Scientifico), S. Gerber(Inserm), Sila Hopton(Newcastle University), Holger Prokisch(Helmholtz Zentrum München), Catherine Vignal‐Clermont, Jean‐Michel Rozet(Inserm), Céline Bris(Université d'Angers), Andrea Legati(Fondazione IRCCS Istituto Neurologico Carlo Besta), Roshni Vara(Evelina London Children's Healthcare), Patrizia Amati‐Bonneau(Inserm), Daniele Ghezzi(University of Milan), Neda Mazaheri(Shahid Chamran University of Ahvaz), Dominique Bonneau(Centre Hospitalier Universitaire d'Angers), Isabella Moroni(Vita-Salute San Raffaele University), Josseline Kaplan(Inserm), Melania Giannotta(Institute of Neurological Sciences), Reza Maroofian(University College London), Gholamreza Shariati(Ahvaz Jundishapur University of Medical Sciences), Robert W. Taylor(Charles Darwin University), Stéphanie Leruez(Université d'Angers), Christine Makowski(Technical University of Munich), Christian P. Hamel(Inserm), Xavier Zanlonghi(Clinique Jules Verne), Steven Hardy(University of Newcastle Australia), Tim M. Strom(Ludwig-Maximilians-Universität München), Tobias B. Haack(Technical University of Munich)
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