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A CACNB4 mutation shows that altered Cav2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy
Iori Ohmori, Mamoru Ouchida, Takafumi Miki, Nobuyoshi Mimaki, Shigeki Kiyonaka, Tei-ichi Nishiki, Kazuhito Tomizawa, Yasuo Mori, Hideki Matsui
Research output: Contribution to journal › Article › peer-review
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(Scopus)