검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome Fendri-Kriaa N, Boujilbene S, Kammoun F, Mkaouar-Rebai E, Ben Mahmoud A, Hsairi I, Rebai A, Triki C, Fakhfakh F Biochemical and Biophysical Research Communications, 408(4), 654, 2011 |
| 2 |
A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene Fendri-Kriaa N, Hsairi I, Kifagi C, Ellouze E, Mkaouar-Rebai E, Triki C, Fakhfakh F Biochemical and Biophysical Research Communications, 409(2), 270, 2011 |