Aberrant White Matter Microstructure in Children and Adolescents With the Subtype of Prader–Willi Syndrome at High Risk for Psychosis

Prader–Willi Syndrome (PWS) is a complex neurogenetic disorder caused by loss of the paternal 15q11.2–q13 locus, due to deletion (DEL), maternal uniparental disomy (mUPD), or imprinting center defects. Individuals with mUPD have up to 60% risk of developing psychosis in early adulthood. Given the in...

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Detalhes bibliográficos
Publicado no:Schizophr Bull
Main Authors: Lukoshe, Akvile, van den Bosch, Gerbrich E, van der Lugt, Aad, Kushner, Steven A, Hokken-Koelega, Anita C, White, Tonya
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2017
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5581891/
https://ncbi.nlm.nih.gov/pubmed/28510708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/schbul/sbx052
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