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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Vydáno v:Schizophr Bull
Hlavní autoři: Lukoshe, Akvile, van den Bosch, Gerbrich E, van der Lugt, Aad, Kushner, Steven A, Hokken-Koelega, Anita C, White, Tonya
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2017
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Regular Articles
On-line přístup: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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