검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A > G and the ND1 m.3308T > C mutations associated with multiple mitochondrial deletions Mezghani N, Mnif M, Mkaouar-Rebai E, Kallel N, Charfi N, Abid M, Fakhfakh F Biochemical and Biophysical Research Communications, 431(4), 670, 2013 |
| 2 |
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 |