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
收藏
页码：842 / 843
页数：2
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