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Neurology, Vol. 68, Issue 19, 1553-1554, May 8, 2007

EDITORIALS

Clinical heterogeneity of ATP13A2 linked disease (Kufor-Rakeb) justifies a PARK designation

Andrew J. Lees and Andrew B. Singleton

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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. Martignoni, L. Lopiano, L. B. Jardim, B. A. Oostra, E. R. Barbosa, The Italian Parkinson Genetics Network, and V. Bonifati
Neurology 2007 68: 1557-1562. [Abstract] [Full Text] [PDF]




This Article
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PubMed
Right arrow Articles by Lees, A. J.
Right arrow Articles by Singleton, A. B.
Related Collections
Right arrow All Movement Disorders
Right arrow Parkinson's disease/Parkinsonism
Right arrow Parkinson's disease with dementia
Right arrow All Genetics
Right arrowRelated Article