SPECTRUM OF SCN1A GENE MUTATIONS IN PATIENTS WITH DRAVET SYNDROME AND RELATED TO INFANTILE EPILEPTIC ENCEPHALOPATHIES

被引：0

作者：

Heberle, C. ^{[1
]}

Mayer, K. ^{[1
]}

Rost, I. ^{[1
]}

机构：

[1] Ctr Human Genet & Lab Med, Martinsried, Germany

来源：

EPILEPSIA | 2010年 / 51卷

关键词：

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：

引用

页码：33 / 33

页数：1

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