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

✍ Scribed by Winkelmann, J.; Lin, L.; Schormair, B.; Kornum, B. R.; Faraco, J.; Plazzi, G.; Melberg, A.; Cornelio, F.; Urban, A. E.; Pizza, F.; Poli, F.; Grubert, F.; Wieland, T.; Graf, E.; Hallmayer, J.; Strom, T. M.; Mignot, E.

Book ID: 125441457
Publisher: Oxford University Press
Year: 2012
Tongue: English
Weight: 340 KB
Volume: 21
Category: Article
ISSN: 0964-6906
DOI: 10.1093/hmg/dds035

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