Accepted Article Expanding the histopathological spectrum of CFL2-related myopathies Short running title: Congenital myopathy related to new CFL2 mutations Fabiana Fattori 1 , Chiara Fiorillo 2 , Carmelo Rodolico 3 , Giorgio Tasca 4 , Margherita Verardo 1 , Emanuele Bellacchio 5 , Simone Pizzi 5 , Andrea Ciolfi 5 , Gigliola Fagiolari 6 , Antonino Lupica 3 , Paolo Broda 2 , Marina Pedemonte 2 , Maurizio Moggio 6 , Claudio Bruno 2 , Marco Tartaglia 5 , Enrico Bertini 1,5 , Adele D’Amico 1 1 Neuromuscular Diseases, Genetics and Rare Diseases Research Division, Bambino Gesù Children’s Hospital, Rome, Italy; 2 Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy; 3 Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy; 4 Istituto di Neurologia, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario "A. Gemelli", Rome; 5 Molecular Genetics and Functional Genomics, Genetics and Rare Diseases Research Division, Bambino Gesù Children’s Hospital, Rome, Italy; 6 Neuromuscular and Rare Disease Unit, Department of Neuroscience, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy. Corresponding Author: Adele D’Amico, Unit of Muscular and Neurodegenerative diseases, Bambino Gesù Children’s Hospital, Viale San Paolo 15, 0146 Rome Italy; Phone number: +390668592105 e-mail address: adele2.damico@opbg.net Conflict of interest statement: none This article is protected by copyright. All rights reserved. This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1111/cge.13240