Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array
Language: English
Page range: 5 - 13
Submitted on: May 24, 2012
|Accepted on: Jun 3, 2013
|Published on: Jun 10, 2013
Published by: The Foundation of Epileptology
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2013 Takayuki Sugawara, Shuichi Yoshida, Naoko Onodera, Kazumaru Wada, Shinichi Hirose, Sunao Kaneko, published by The Foundation of Epileptology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.