Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
Winkelmann J; Lin L; Schormair B; Kornum BR; Faraco J; Plazzi G; Melberg A; Cornelio F; Urban AE; Pizza F; Poli F; Grubert F; Wieland T; Graf E; Hallmayer J; Strom TM; Mignot E; Human Molecular Genetics, 2012, vol. 21, issue 10, p 2205, ISSN 14602083. ISBN 14602083.

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