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Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array
Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array
2013
Takayuki Sugawara
Shuichi Yoshida
Naoko Onodera
Kazumaru Wada
Shinichi Hirose
Sunao Kaneko
Keywords:
Psychiatry
Epilepsy
Pediatrics
Medicine
Myoclonic epilepsy
in patient
Correction
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