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
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R74 [神经病学与精神病学];
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页码：33 / 33
页数：1
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