New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures

  • New mutation and a putative disease-associated haplotype within SCN1B gene
  • N. Fendri-Kriaa, F. Kammoun, I. Hadj Salem, C. Kifagi, E. Mkaouar-Rebai, I. Hsairi, A. Rebai, C. Triki, F. Fakhfakh
  • European Journal of Neurology, October 2010, Wiley
  • DOI: 10.1111/j.1468-1331.2010.03216.x

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http://dx.doi.org/10.1111/j.1468-1331.2010.03216.x

The following have contributed to this page: Dr Ahmed Rebai