Fr Ar
New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures. Eur J Neurol. 18: 695-702
de Fendri-Kriaa N, Kammoun F., Salem IH., Kifagi C., Mkaouar-Rebai E., Hsairi I.,Rebai A., Triki C., Fakhfakh F
2011

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