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2. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia. Le Ber I, Clot F, Vercueil L, Camuzat A, Viémont M, Benamar N, De Liège P, Ouvrard-Hernandez AM, Pollak P, Stevanin G, Brice A, Dürr A. Neurology; 2006 Nov 28; 67(10):1769-73. PubMed ID: 17130408 [Abstract] [Full Text] [Related]
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