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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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Hlavní autoři: Kusenda, M., Sebat, J.
Médium: Artigo
Jazyk:Inglês
Vydáno: S. Karger AG 2009
Témata:
On-line přístup: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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