ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

A. Di Fonzo, H. F. Chien, M. Socal, S. Giraudo, C. Tassorelli, G. Iliceto, G. Fabbrini, R. Marconi, E. Fincati, G. Abbruzzese, P. Marini, F. Squitieri, M. W. Horstink, P. Montagna, A. Dalla Libera, F. Stocchi, S. Goldwurm, J. J. Ferreira, G. Meco, E. MartignoniL. Lopiano, L. B. Jardim, B. A. Oostra, E. R. Barbosa, V. Bonifati, V. Bonifati, N. Vanacore, G. Meco, G. Fabbrini, E. Fabrizio, N. Locuratolo, C. Scoppetta, M. Manfredi, A. Berardelli, L. Lopiano, S. Giraudo, B. Bergamasco, C. Tassorelli, C. Pacchetti, G. Nappi, S. Goldwurm, A. Antonini, G. Pezzoli, G. Riboldazzi, G. Bono, F. Raudino, Mi Manfredi, E. Fincati, M. Tinazzi, A. Bonizzato, C. Ferracci, A. Dalla Libera, G. Abbruzzese, R. Marchese, P. Montagna, P. Marini, F. Massaro, R. Marconi, M. Guidi, C. Minardi, F. Rasi, M. Onofrj, A. Thomas, F. Stocchi, L. Vacca, F. De Pandis, M. De Mari, C. Diroma, G. Iliceto, P. Lamberti, V. Toni, G. Trianni, A. Mauro, A. De Gaetano, M. Rizzo, G. Cossu, Carlos R M Rieder, Maria Luiza Saraiva-Pereira

Research output: Contribution to journalArticlepeer-review

Abstract

OBJECTIVE: To assess the prevalence, nature, and associated phenotypes of ATP13A2 gene mutations among patients with juvenile parkinsonism (onset

Original languageEnglish
Pages (from-to)1557-1562
Number of pages6
JournalNeurology
Volume68
Issue number19
DOIs
Publication statusPublished - May 2007

ASJC Scopus subject areas

  • Neuroscience(all)

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