검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening Alila-Fersi O, Chamkha I, Majdoub I, Gargouri L, Mkaouar-Rebai E, Tabebi M, Tlili A, Keskes L, Mahfoudh A, Fakhfakh F Biochemical and Biophysical Research Communications, 484(1), 71, 2017 |
| 2 |
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 |