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Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy

✍ Scribed by Wang, Ji-wen; Shi, Xiu-yu; Kurahashi, Hirokazu; Hwang, Su-Kyeong; Ishii, Atsushi; Higurashi, Norimichi; Kaneko, Sunao; Hirose, Shinichi

No coin nor oath required. For personal study only.

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