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Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array Cover

Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array

Open Access
|Jun 2013

References

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DOI: https://doi.org/10.21307/joepi-2015-0001 | Journal eISSN: 2299-9728 | Journal ISSN: 2300-0147
Language: English
Page range: 5 - 13
Submitted on: May 24, 2012
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Accepted on: Jun 3, 2013
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Published on: Jun 10, 2013
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 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.