Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?

Iori Ohmori, Yoko Ohtsuka, Mamoru Ouchida, Tatsuya Ogino, Satoshi Maniwa, Kenji Shimizu, Eiji Oka

Research output: Contribution to journalArticlepeer-review

39 Citations (Scopus)

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Medicine & Life Sciences