Phenotypic Variability In Rett Patients With Mecp2 Mutations: Clinical, Molecular And Computational Analysis

被引：0
|
作者：
Kharrat, M. [1 ]
Kamoun, F. [2 ]
Triki, C. [2 ]
Faiza, F. [1 ]
机构：
[1] Univ Sfax, Fac Sci Sfax, Lab Mol & Funct Genet, Sfax, Tunisia
[2] CHU Hedi Chaker Sfax, Serv Neurol Infantile, Sfax, Tunisia
来源：
EPILEPSIA | 2018年 / 59卷
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D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
p429
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页码：S197 / S197
页数：1
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