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About this Biochemistry, Genetics and Molecular Biology article
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy 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. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- 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.
- Publisher
- Oxford University Press; Oxford University Press (OUP) (ISSN 0964-6906)
- Published
- 2012
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)