DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Sahli M, Zrhidri A, Elaloui SC. et al.
Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series.
J Med Case Reports 2019;
13 (01) 266
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