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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
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2012 (English)In: Sleep, ISSN 0161-8105, E-ISSN 1550-9109, Vol. 35, no S, A11-A11 p.Article in journal, Meeting abstract (Other academic) Published
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2012. Vol. 35, no S, A11-A11 p.
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Medical and Health Sciences
URN: urn:nbn:se:uu:diva-193726ISI: 000312996500024OAI: oai:DiVA.org:uu-193726DiVA: diva2:603465
Annual Meeting of the Associated-Professional-Sleep-Societies (APSS), JUN 09-13, 2012, Boston, MA, USA
Available from: 2013-02-06 Created: 2013-02-06 Last updated: 2013-02-06Bibliographically approved

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