검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
A novel mutation MT-COIII m.9267G > C and MT-COI m.5913G > A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy Tabebi M, Mkaouar-Rebai E, Mnif M, Kallabi F, Ben Mahmoud A, Ben Saad W, Charfi N, Keskes-Ammar L, Kamoun H, Abid M, Fakhfakh F Biochemical and Biophysical Research Communications, 459(3), 353, 2015 |
| 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 |