DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

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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