DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Ogiwara I, Nakayama T, Yamagata T , et al.
A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.
Epilepsia 2012;
53 (12) e200-e203
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