Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia

Prader-Willi Syndrome (PWS) is a neurodevelopmental disorder caused by mutations affecting paternal chromosome 15q11-q13, and characterized by hypotonia, hyperphagia, impaired cognition, and behavioural problems. Psychotic illness is a challenging problem for individuals with PWS and has different r...

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Detalles Bibliográficos
Autores principales: Zahova, Simona K., Humby, Trevor, Davies, Jennifer R., Morgan, Joanne E., Isles, Anthony R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379171/
https://www.ncbi.nlm.nih.gov/pubmed/34417445
http://dx.doi.org/10.1038/s41398-021-01561-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379171/
https://www.ncbi.nlm.nih.gov/pubmed/34417445
http://dx.doi.org/10.1038/s41398-021-01561-x

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