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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

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Description scientific article
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author: Fabio Pizza  Emmanuel Mignot  Giuseppe Plazzi  Juliane Winkelmann  Juliette Faraco  Birgitte Rahbek Kornum  Joachim Hallmayer  Tim M Strom  Barbara Schormair  Ferdinando Cornelio  Francesca Poli 

Publication date February 9, 2012
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