(Q28290069)
Statements
Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort (English)
Hirokazu Oguni
Kitami Hayashi
Makiko Osawa
Yutaka Awaya
Yukio Fukuyama
Goryu Fukuma
Shinichi Hirose
Akihisa Mitsudome