A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia (Q24337555)

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A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia
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    A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia (English)
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    Niccolo E Mencacci
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    Anselm Zdebik
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    Ann-Kathrin Hauser
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    Sara Bandres-Ciga
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    Conceição Bettencourt
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    Paola Forabosco
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    Deborah Hughes
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    Marc M P Soutar
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    Mehmet Tekman
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    Horia C Stanescu
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    Robert Kleta
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    Miryam Carecchio
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    Giovanna Zorzi
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    Ebba Lohmann
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    Anne Weissbach
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    Thomas Gasser
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    4 June 2015
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    96
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    6
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    938-47
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