Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy

doi:10.1111/j.1528-1167.2008.01549_2.x

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Wiley InterScience

Epilepsia

Volume 49 Issue 6, Pages 1104 - 1107

Published Online: 4 Jun 2008

Published on behalf of the International League Against Epilepsy (ILAE)

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Letters/Commentary

Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy

Huihui Sun ¹ Yuehua Zhang ¹ zhangyhd@hotmail.com Jianmin Liang ^1,2 Xiaoyan Liu ¹ Xiuwei Ma ¹ Jiong Qin ¹ Yu Qi ¹ Xiru Wu ¹

¹ Department of Pediatrics
Peking University, First Hospital, Beijing
100034, P. R. China
² Department of Pediatrics
Jilin University, First Hospital
Changchun, 130021, China