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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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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
S. Karger AG
2009
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| Matèries: | |
| Accés en línia: | 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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