The first familial case with the entire CNKSR2 gene deletion corroborating its involvement in X-linked intellectual disability and Attention-Deficit/Hyperactivity Disorder (ADHD)

被引：0
|
作者：
Harbuz, Radu [1 ]
Gilbert-Dussardier, Brigitte [1 ]
Couet, Dominique [1 ]
Dumaine, Patricia [1 ]
Kitzis, Alain [1 ]
Bilan, Frederic [1 ]
机构：
[1] CHU Poitiers, Serv Genet, Poitiers, France
来源：
CHROMOSOME RESEARCH | 2013年 / 21卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
1.P36
引用
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页码：S49 / S49
页数：1
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