We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.AuthorsWinkelmann, Juliane; Lin, Ling; Schormair, Barbara; Kornum, Birgitte R.; Faraco, Juliette; Plazzi, Giuseppe; Melberg, Atle; Cornelio, Ferdinando; Urban, Alexander E.; Pizza, Fabio; Poli, Francesca; Grubert, Fabian; Wieland, Thomas; Graf, Elisabeth; Hallmayer, Joachim; Strom, Tim M.; Mignot, EmmanuelPublicationHuman Molecular Genetics, 2012, Vol 21, Issue 10, p2205ISSN0964-6906Publication typearticleDOI10.1093/hmg/dds035