Grey matter volume and cortical structure in Prader-Willi syndrome compared to typically developing young adults

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with a characteristic overeating disorder, mild to moderate intellectual disability, and a variable range of social and behavioral difficulties. Consequently, widespread alterations in neural structure and...

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Detalles Bibliográficos
Autores principales: Manning, Katherine E., Tait, Roger, Suckling, John, Holland, Anthony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842730/
https://www.ncbi.nlm.nih.gov/pubmed/29527494
http://dx.doi.org/10.1016/j.nicl.2017.12.027

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842730/
https://www.ncbi.nlm.nih.gov/pubmed/29527494
http://dx.doi.org/10.1016/j.nicl.2017.12.027

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