검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
A whole mitochondrial genome screening in a MELAS patient: A novel mitochondrial tRNA(Val) mutation Mezghani N, Mnif M, Kacem M, Mkaouar-Rebai E, Salem IH, Kallel N, Charfi N, Abid M, Fakhfakh F Biochemical and Biophysical Research Communications, 407(4), 747, 2011 |
| 2 |
MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation Connolly BS, Feigenbaum ASJ, Robinson BH, Dipchand AI, Simon DK, Tarnopolsky MA Biochemical and Biophysical Research Communications, 402(2), 443, 2010 |