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Dive into the research topics of 'Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy'. Together they form a unique fingerprint.- Sort by
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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