Detection of SCN1A mutations in patients with severe...

Journal of Epileptology 2013 / 01 Vol. 21; Iss. 1

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

Sugawara, Takayuki, Yoshida, Shuichi, Onodera, Naoko, Wada, Kazumaru, Hirose, Shinichi, Kaneko, Sunao
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Volume:
21
Language:
english
Journal:
Journal of Epileptology
DOI:
10.1515/joepi-2015-0001
Date:
January, 2013
File:
PDF, 953 KB
english, 2013
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