Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader–Willi syndrome: A comparison between maternal uniparental disomy and deletion cases

This study aims to compare maternal uniparental disomy 15 (mUPD) and a paternal deletion of 15q11-13 (DEL) of Prader–Willi syndrome (PWS) in regard to autism spectrum disorders (ASD). Forty-five Japanese individuals with PWS were recruited from a single recruitment center. The participants consisted...

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Detalhes bibliográficos
Publicado no:Am J Med Genet A
Main Authors: Ogata, Hiroyuki, Ihara, Hiroshi, Murakami, Nobuyuki, Gito, Masao, Kido, Yasuhiro, Nagai, Toshiro
Formato: Artigo
Idioma:Inglês
Publicado em: BlackWell Publishing Ltd 2014
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4278412/
https://ncbi.nlm.nih.gov/pubmed/24850752
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.36615
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