Schizophrenia: Genome, interrupted

被引：18

作者：

Cantor, Rita M. ^{[1
,2
]}

Geschwind, Daniel H. ^{[1
,2
,3
]}

机构：

[1] Univ Calif Los Angeles, Dept Human Genet, David Geffen Sch Med, Los Angeles, CA 90095 USA

[2] Univ Calif Los Angeles, Ctr Neurobehav Genet, Semel Inst, Los Angeles, CA 90095 USA

[3] Univ Calif Los Angeles, Program Neurogenet, Dept Neurol, Los Angeles, CA 90095 USA

来源：

NEURON | 2008年 / 58卷 / 02期

关键词：

D O I：

10.1016/j.neuron.2008.04.007

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

Structural chromosomal variation is increasingly recognized as an important contributor to human diseases, particularly those of neurodevelopment, such as autism. A current paper makes a significant advance to schizophrenia genetics by establishing an association with rare copy number variants (CNV), which are over-represented in neurodevelopmental genes.

引用

页码：165 / 167

页数：3

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