검색결과 : 3건
| No. | Article |
|---|---|
| 1 |
First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy Alila-Fersi O, Tabebi M, Maalej M, Belguith N, Keskes L, Mkaouar-Rebai E, Fakhfakh F Biochemical and Biophysical Research Communications, 497(4), 1049, 2018 |
| 2 |
First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation Ghorbel R, Ghorbel R, Rouissi A, Fendri-Kriaa N, Ben Salah G, Belguith N, Ammar-Keskes L, Gouider-Khouja N, Fakhfakh F Biochemical and Biophysical Research Communications, 497(1), 93, 2018 |
| 3 |
Mutational analysis of the mitochondrial tRNA(Leu(UUR)) gene in Tunisian patients with mitochondrial diseases Mkaouar-Rebai E, Tlili A, Masmoudi S, Belguith N, Charfeddine I, Mnif M, Triki C, Fakhfakh F Biochemical and Biophysical Research Communications, 355(4), 1031, 2007 |