Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome

STUDY OBJECTIVES: Sleep-wake disturbances are often reported in Prader-Willi syndrome (PWS), a rare neurodevelopmental syndrome that is associated with paternally-expressed genomic imprinting defects within the human chromosome region 15q11-13. One of the candidate genes, prevalently expressed in th...

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Dades bibliogràfiques
Publicat a:Sleep
Autors principals: Lassi, Glenda, Priano, Lorenzo, Maggi, Silvia, Garcia-Garcia, Celina, Balzani, Edoardo, El-Assawy, Nadia, Pagani, Marco, Tinarelli, Federico, Giardino, Daniela, Mauro, Alessandro, Peters, Jo, Gozzi, Alessandro, Grugni, Graziano, Tucci, Valter
Format: Artigo
Idioma:Inglês
Publicat: Associated Professional Sleep Societies, LLC 2016
Matèries:
Basic Science
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4763347/
https://ncbi.nlm.nih.gov/pubmed/26446116
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5665/sleep.5542
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