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

✍ Scribed by N. Fendri-Kriaa; F. Kammoun; I. Hadj Salem; C. Kifagi; E. Mkaouar-Rebai; I. Hsairi; A. Rebai; C. Triki; F. Fakhfakh


Book ID
111066538
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
497 KB
Volume
18
Category
Article
ISSN
1351-5101

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