Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome
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Title
Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome
Authors
Keywords
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Journal
SLEEP
Volume 39, Issue 3, Pages 637-644
Publisher
Oxford University Press (OUP)
Online
2016-03-01
DOI
10.5665/sleep.5542
References
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Note: Only part of the references are listed.- Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome
- (2014) Eric Bieth et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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- (2010) Feng Ding et al. PLoS One
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- (2009) Kurt Krauchi Frontiers in Bioscience-Landmark
- A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism
- (2009) A. J. de Smith et al. HUMAN MOLECULAR GENETICS
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- (2009) Evgueniy V. Lubenov et al. NATURE
- A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome
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- (2008) Alun R. Barnard et al. PLoS Genetics
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