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Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28
2010
341 citations
Journal Article
Field-Weighted Citation Impact:
11.28
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28 | Researchclopedia
Claudia Cagnoli
·
University of Turin
Filippo Tempia
·
Neuroscience Institute
Marina Frontali
·
Institute of Neurobiology and Molecular Medicine
Liana Veneziano
·
Institute of Neurobiology and Molecular Medicine
Tiziana Sacco
·
Neuroscience Institute
Enrica Boda
·
Neuroscience Institute
Alessandro Brussino
·
University of Turin
Florian Bonn
·
University of Cologne
Barbara Castellotti
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Silvia Baratta
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Caterina Mariotti
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Cinzia Gellera
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Valentina Fracasso
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Stefania Magri
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Thomas Langer
·
University of Cologne
Paolo Plevani
·
University of Milan
Stefano Di Donato
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Marco Muzi-Falconi
·
University of Milan
Franco Taroni
·
Fondazione IRCCS Istituto Neurologico Carlo Besta