Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders
Paola Borgia(Istituto Giannina Gaslini), Vincenzo Salpietro(University College London), Ebba Alkhunaizi(University of Toronto), Miguel A. Soler(Italian Institute of Technology), Andrea Accogli(Istituto Giannina Gaslini), Sımona Baldassari(Istituto Giannina Gaslini), Shima Imannezhad(Mashhad University of Medical Sciences), Mohammad Hasan Mohammadi(Zabol University of Medical Sciences), Domenico Tortora(Istituto Giannina Gaslini), Mohamad Maghnie(Istituto Giannina Gaslini), Paolo Scudieri(Istituto Giannina Gaslini), Mehran Beiraghi Toosi(Mashhad University of Medical Sciences), Ilaria Musante(Istituto Giannina Gaslini), Elisa Calì(National Hospital for Neurology and Neurosurgery), Gianluca D’Onofrio(Centre Hospitalier Universitaire Sainte-Justine), Maria Stella Vari(Istituto Giannina Gaslini), Ganna Balagura(University of Genoa), Farah Ashrafzadeh(Mashhad University of Medical Sciences), Michele Iacomino(Istituto Giannina Gaslini), Roberto Chimenz(Unknown), Sara Fortuna(University of Trieste), Nicoletta Pedemonte(Istituto Giannina Gaslini), Antonella Riva(University of Genoa), Federico Zara(Istituto Giannina Gaslini), Giuseppe Donato Mangano(University of Palermo), Marina Pedemonte(Istituto Giannina Gaslini), Ehsan Ghayoor Karimiani(St George's, University of London), Chiara Fiorillo(Fondazione Stella Maris), Henry Houlden(University College London), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Pasquale Striano(Great Ormond Street Hospital), Maria Cristina Schiaffino(University of Genoa), Karl Echiverri(University of Kentucky), Maria Cristina Diana(Istituto Giannina Gaslini), Charles K. Abrams(University of Illinois Chicago)
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