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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...
Autores principales: | Bennett, Jeffrey A., Hodgetts, Sandra, Mackenzie, Michelle L., Haqq, Andrea M., Zwaigenbaum, Lonnie |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
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 |
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