ALTERED MOLECULAR PHENOTYPES IN 22Q DELETION SYNDROME

被引：0

作者：

Tassone, F. ^{[1
,2
]}

Kooy, F. ^{[3
]}

Girirajan, S. ^{[4
]}

Simon, T. ^{[2
,5
]}

机构：

[1] Univ Calif Davis, Sch Med, Dept Biochem & Mol Med, Davis, CA 95616 USA

[2] Univ Calif Davis, Med Ctr, MIND Inst, Davis, CA 95616 USA

[3] Univ Antwerp, Dept Biomed Sci, Antwerp, Belgium

[4] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA

[5] Univ Calif Davis, Sch Med, Dept Psychiat, Davis, CA 95616 USA

来源：

JOURNAL OF INTELLECTUAL DISABILITY RESEARCH | 2016年 / 60卷 / 09期

关键词：

22q deletion; CNV; miRNA; mitochondrial dysfunction; intellectual disabilities;

D O I：

暂无

中图分类号：

G76 [特殊教育];

学科分类号：

040109 ;

摘要：

引用

页码：842 / 843

页数：2

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