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

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44 Citations (Scopus)

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