Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, New York 11724, USA.
Nat Rev Genet. 2014 Feb;15(2):133-41. doi: 10.1038/nrg3585. Epub 2014 Jan 16.
The identification of the genetic components of autism spectrum disorders (ASDs) has advanced rapidly in recent years, particularly with the demonstration of de novo mutations as an important source of causality. We review these developments in light of genetic models for ASDs. We consider the number of genetic loci that underlie ASDs and the relative contributions from different mutational classes, and we discuss possible mechanisms by which these mutations might lead to dysfunction. We update the two-class risk genetic model for autism, especially in regard to children with high intelligence quotients.
近年来,自闭症谱系障碍(ASD)的遗传成分的鉴定取得了快速进展,特别是新发现的突变被证明是因果关系的一个重要来源。我们根据 ASD 的遗传模型来回顾这些进展。我们考虑了 ASD 所涉及的遗传基因座的数量以及不同突变类别相对的贡献,并讨论了这些突变可能导致功能障碍的可能机制。我们更新了自闭症的两类别风险遗传模型,特别是对于高智商的儿童。