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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...
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| 出版年: | Int J Mol Sci |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5372533/ https://ncbi.nlm.nih.gov/pubmed/28264487 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18030517 |
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