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

Juliane Winkelmann, Ling Lin, Barbara Schormair, Birgitte R. Kornum, Juliette Faraco, Giuseppe Plazzi, Atle Melberg, Ferdinando Cornelio, Alexander E. Urban, Fabio Pizza, Francesca Poli, Fabian Grubert, Thomas Wieland, Elisabeth Graf, Joachim Hallmayer, Tim M. Strom, Emmanuel Mignot

Research output: Contribution to journal › Article › peer-review

209 Scopus citations

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Neuroscience