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Mutations in DNMT1 cause autosomal dominant cerebellar at... | ResearchHub
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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
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Authors
Juliane Winkelmann
16 more
Juliane Winkelmann
•
Ling Lin
14 more
•
Emmanuel Mignot
Published
February 9, 2012
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Journal
Human Molecular Genetics
Topics
Biology
Neuroscience
Neurology
Genetics
Cognitive Neuroscience
Show all topics
DOI
10.1093/hmg/dds035
