검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders Mkaouar-Rebai E, Felhi R, Tabebi M, Alila-Fersi O, Chamkha I, Maalej M, Ammar M, Kammoun F, Keskes L, Hachicha M, Fakhfakh F Biochemical and Biophysical Research Communications, 473(2), 578, 2016 |
| 2 |
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 |