DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Wang JW, Shi XY, Kurahashi H. et al; Epilepsy Genetic Study Group Japan.
Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.
Epilepsy Res 2012;
102 (03) 195-200
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