Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
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author: Birgitte Rahbek Kornum, Juliane Winkelmann, Giuseppe Plazzi, Fabio Pizza, Emmanuel Mignot, Juliette Faraco, Ferdinando Cornelio, Tim M Strom, Francesca Poli, Barbara Schormair, Joachim Hallmayer
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