Puzzle Pieces: Neural Structure and Function in Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with a behavioural phenotype encompassing hyperphagia, intellectual disability, social and behavioural difficulties, and propensity to psychiatric illness. Research has tended to focus on the cognitive and...

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Detalles Bibliográficos
Autores principales: Manning, Katherine E., Holland, Anthony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548261/
https://www.ncbi.nlm.nih.gov/pubmed/28943631
http://dx.doi.org/10.3390/diseases3040382

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548261/
https://www.ncbi.nlm.nih.gov/pubmed/28943631
http://dx.doi.org/10.3390/diseases3040382

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