Open Access
Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array
Takayuki Sugawara/ Shuichi Yoshida/ Naoko Onodera/ Kazumaru Wada/ Shinichi Hirose/ Sunao Kaneko
DOI: 10.1515/joepi-2015-0001
Published Online: 10-June-2013