Genome Variation and Complexity in the Autism Spectrum

被引：10
|
作者：
van de Lagemaat, L. N. [1 ]
Grant, Seth G. N. [1 ]
机构：
[1] Wellcome Trust Sanger Inst, Genes Cognit Programme, Hinxton CB10 1SA, Cambs, England
来源：
NEURON | 2010年 / 67卷 / 01期
关键词：
WIDE ASSOCIATION; SCHIZOPHRENIA; MUTATIONS;
D O I：
10.1016/j.neuron.2010.06.026
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
A large international consortium reports in Nature on the diversity of genomic changes in families with autism spectrum disorders. Inherited and de novo mutations affecting many genes were discovered implicating disruption to postsynaptic and cellular signaling processes.
引用
收藏
页码：8 / 10
页数：3
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