In response: SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability

Affiliations

¹ Department of Pediatrics, Peking University First Hospital, Beijing, China.
² Department of Pediatrics, Peking University First Hospital, Beijing, China. jiangyuwu@bjmu.edu.cn.

Comment

Weijing Kong et al. Epilepsia. 2015 Aug.

. 2015 Aug;56(8):1320.

doi: 10.1111/epi.13059.

¹ Department of Pediatrics, Peking University First Hospital, Beijing, China.
² Department of Pediatrics, Peking University First Hospital, Beijing, China. jiangyuwu@bjmu.edu.cn.

No abstract available

Comment on

SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability.
Kong W, Zhang Y, Gao Y, Liu X, Gao K, Xie H, Wang J, Wu Y, Zhang Y, Wu X, Jiang Y. Kong W, et al. Epilepsia. 2015 Mar;56(3):431-8. doi: 10.1111/epi.12925. Epub 2015 Feb 26. Epilepsia. 2015. PMID: 25785782
SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability.
Fung LW, Kwok SL, Tsui KW. Fung LW, et al. Epilepsia. 2015 Aug;56(8):1319-20. doi: 10.1111/epi.13016. Epilepsia. 2015. PMID: 26235738 No abstract available.