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Article

Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.

Advances in neurology - 1 Jan 2005

Oguni Hirokazu, Hayashi Kitami, Osawa Makiko, Awaya Yutaka, Fukuyama Yukio, Fukuma Goryu, Hirose Shinichi, Mitsudome Akihisa, Kaneko Sunao

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PMID: 15508916

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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