Cognitive deficits in the Snord116 deletion mouse model for Prader-Willi syndrome

Prader-Willi syndrome (PWS) is an imprinted neurodevelopmental disease caused by a loss of paternal genes on chromosome 15q11-q13. It is characterized by cognitive impairments, developmental delay, sleep abnormalities, and hyperphagia often leading to obesity. Clinical research has shown that a lack...

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Vydáno v:Neurobiol Learn Mem
Hlavní autoři: Adhikari, Anna, Copping, Nycole A., Onaga, Beth, Pride, Michael C., Coulson, Rochelle L., Yang, Mu, Yasui, Dag H., LaSalle, Janine M., Silverman, Jill L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2018
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6520209/
https://ncbi.nlm.nih.gov/pubmed/29800646
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nlm.2018.05.011
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