Mutation at the SCA17 locus is not a common cause of primary dystonia

By Grundmann Kathrin   Laubis-Herrmann Ulrike   Dressler Dirk   Vollmer-Haase Juliane   Bauer Peter   Stuhrmann Manfred   Schulte Thorsten   Schöls Ludger   Topka Helge   Riess Olaf  

Journal of Neurology, Vol. 251, Iss. 10, 2004-10 ,pp. : 1232-1234

Springer Publishing Company

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Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation

By Boeve Bradley F.  

Brain, Vol. 128, Iss. 4, 2005-04 ,pp. : 752-772

Oxford University Press

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Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation

By Baba Y.   Baker M. C.   Le Ber I.   Brice A.   Maeck L.   Kohlhase J.   Yasuda M.   Stoppe G.   Bugiani O.   Sperfeld A. D.   Tsuboi Y.   Uitti R. J.   Farrer M. J.   Ghetti B.   Hutton M. L.   Wszolek Z. K.  

Journal of Neural Transmission, Vol. 114, Iss. 7, 2007-07 ,pp. : 947-950

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Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)

By Lasek K.   Lencer R.   Gaser C.   Hagenah J.   Walter U.   Wolters A.   Kock N.   Steinlechner S.   Nagel M.   Zühlke C.   Nitschke M.-F.   Brockmann K.   Klein C.   Rolfs A.   Binkofski F.  

Brain, Vol. 129, Iss. 9, 2006-09 ,pp. : 2341-2352

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The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's disease

By Winkler Susen   Vollstedt Eva-Juliane   Kasten Meike   Alvarez-Fischer Daniel   Klein Christine   Lohmann Katja  

Journal of Neurology, Vol. 261, Iss. 4, 2014-04 ,pp. : 833-834

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