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Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.
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Publications
Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.
Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.
Hirokazu Oguni
Hirokazu Oguni
Kitami Hayashi
Kitami Hayashi
Makiko Osawa
Makiko Osawa
YA
Yutaka Awaya
Yutaka Awaya
YF
Yukio Fukuyama
Yukio Fukuyama
GF
Goryu Fukuma
Goryu Fukuma
Shinichi Hirose
Shinichi Hirose
AM
Akihisa Mitsudome
Akihisa Mitsudome
SK
Sunao Kaneko
Sunao Kaneko
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1 January 2005
journal article
case report
Vol. 95
,
103-17
Abstract
No abstract available
Cited by 14 articles