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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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| Publicado no: | Neurobiol Learn Mem |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | 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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