Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to overexpression of the MECP2 gene

被引：0
|
作者：
Vieira, J. P. [1 ]
Silva-Fernandes, A. [2 ]
Moura, S. [2 ]
Maciel, P. [2 ]
机构：
[1] Hosp D Estefania, Lisbon, Portugal
[2] Univ Minho, P-4719 Braga, Portugal
来源：
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE | 2010年 / 28卷 / 08期
关键词：
Developmental delay; Epilepsy; Molecular genetics; Mental retardation;
D O I：
10.1016/j.ijdevneu.2010.07.125
中图分类号：
Q [生物科学];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
引用
收藏
页码：683 / 684
页数：2
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