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G蛋白偶联受体37的基因突变与自闭症发病机制相关性的研究 被引量:2

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摘要 泛自闭症障碍症候群(ASD )是一种神经发育障碍性疾病,它的主要特征为交流障碍,社会能力缺失,刻板的兴趣和重复的行为。目前有文献[1-5]报道已经确定了NLGN3、NLGN4、CADM1、CNPNAP2及SHANK3为自闭症的相关性基因。此外,TSC1/2的突变也可能与自闭症相关[6]。但是,这些基因突变导致自闭症的分子机制尚不清楚。
出处 《山西医药杂志(上半月)》 CAS 2014年第2期139-142,共4页 Shanxi Medical Journal
基金 辽宁省科技厅博士科研启动基金(20081060)
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参考文献16

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