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A homozygous mutation of voltage-gated sodium channel β I gene SCN1B in a patient with Dravet syndrome

✍ Scribed by Ogiwara, Ikuo; Nakayama, Tojo; Yamagata, Tetsushi; Ohtani, Hideyuki; Mazaki, Emi; Tsuchiya, Shigeru; Inoue, Yushi; Yamakawa, Kazuhiro

No coin nor oath required. For personal study only.

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