DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

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

Download Bibliographical Data

Search in: