검색결과 : 3건
| No. | Article |
|---|---|
| 1 |
Mitochondrial myopathy in a child with a muscle-restricted mutation in the mitochondrial transfer RNA(Asn) gene Bruno C, Cassandrini D, Fattori F, Pedemonte M, Fiorillo C, Brigati G, Brisca G, Minetti C, Santorelli FM Biochemical and Biophysical Research Communications, 412(4), 518, 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 |
| 3 |
A novel mutation 3090 G > A of the mitochondrial 16S ribosomal RNA associated with myopathy Coulbault L, Deslandes B, Herlicoviez D, Read MH, Leporrier N, Schaeffer S, Mouadil A, Lombes A, Chapon F, Jauzac P, Allouche S Biochemical and Biophysical Research Communications, 362(3), 601, 2007 |