DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Fendri-Kriaa N, Kammoun F, Salem IH. et al.
New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures.
Eur J Neurol 2011;
18 (05) 695-702
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