Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease
Giorgio Casari(Telethon Institute Of Genetics And Medicine), Maurizio De Fusco(Telethon Institute Of Genetics And Medicine), Sonia Ciarmatori(Telethon Institute Of Genetics And Medicine), Massimo Zeviani(Fondazione IRCCS Istituto Neurologico Carlo Besta), Marina Mora(Fondazione IRCCS Istituto Neurologico Carlo Besta), Patricio Fernández‐Silva(Bambino Gesù Children's Hospital), Giuseppe De Michele(Federico II University Hospital), Alessandro Filla(Federico II University Hospital), Sergio Cocozza, R. Marconi(Ospedale Misericordia - Grosseto), A. Dürr(Inserm), Bertrand Fontaine(Inserm), Andrea Ballabio(Vita-Salute San Raffaele University)
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