Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome: A Case Study

Prader-Willi syndrome (PWS), a rare genetic disorder caused by the lack of expression of paternal genes from chromosome 15q11-13, has been investigated for autism spectrum disorder (ASD) symptomatology in various studies. However, previous findings have been variable, and no studies investigating AS...

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Detalles Bibliográficos
Autores principales: Bennett, Jeffrey A., Hodgetts, Sandra, Mackenzie, Michelle L., Haqq, Andrea M., Zwaigenbaum, Lonnie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372533/
https://www.ncbi.nlm.nih.gov/pubmed/28264487
http://dx.doi.org/10.3390/ijms18030517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372533/
https://www.ncbi.nlm.nih.gov/pubmed/28264487
http://dx.doi.org/10.3390/ijms18030517

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