Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort (Q28290069)
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Language | Label | Description | Also known as |
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English | Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort |
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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