Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia (Q57970902)

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Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia
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    Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia (English)
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    I. Le Ber
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    F. Clot
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    A. Camuzat
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    M. Viemont
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    N. Benamar
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    P. De Liege
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    A. M. Ouvrard-Hernandez
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    P. Pollak
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    A. Brice
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    A. Durr
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    27 November 2006
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    67
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    10
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    1769-1773
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