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The role of rare structural variants in the genetics of autism spectrum disorders
Autism is a neurodevelopmental disorder characterized by impaired social interaction and communication and restricted interests and behaviors. Despite high estimates of heritability, genetic causes of ASD have long been elusive, due in part to a high degree of genetic and phenotypic heterogeneity (B...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
S. Karger AG
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2920182/ https://ncbi.nlm.nih.gov/pubmed/19287137 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000184690 |
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