Darnell J., Lodish H., Baltimore D.: Molecular Cell Biology. New York, Scientific American Books, 1986, pp 925-935.
2.
Wilson AC, Cann RL: The recent African genesis of humans. Sci Am1992;266:68-73.
3.
Vigilant L. , Stoneking M., Harpending H., et al: African populations and the evolution of human mitochondrial DNA. Science1991;253:1503-1507.
4.
Hirano M., Pavlakis S.: Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): Current concepts. J Child Neurol1994 ; 9:4-13.
5.
Holt I., Harding A., Morgan-Hughes J.: Deletions of mitochondrial DNA in patients with mitochondrial myopathies . Nature1988; 331:717-719.
6.
Shoffner J., Lott M., Lezza A., et al: Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation. Cell1990;61:931-937.
7.
Silvestri G. , Moraes C., Shanske S., et al: A new mtDNA mutation in the tRNALys gene associated with myoclonic epilepsy and ragged-red fibers (MERRF). Am J Hum Genet1992;51:1213-1217.
8.
Goto Y-i , Nonaka I., Horai S :A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalopathies. Nature1990;348:651-653.
9.
GotoY-i, Nonaka I, Horai S: A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) . Biochem Biophys Acta1991;1097:238-240.
10.
Lertrit P., Noer A., Jean-François M., et al: A new disease-related mutation for mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex 1. Am J Hum Genet1992;51: 457-468.
11.
Moraes C., Ciacci F., Silvestri G., et al: Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA. Neuromusc Disord , in press.
12.
King M., Koga Y., Davidson M., Schon E.: Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNALeu(UUR) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Mol Cell Biol1992;12:480-490.
13.
Tritschler H-J., Medori R.: Mitochondrial DNA alterations as a source of human disorders. Neurology1993;43:280-288.
14.
Stent G.:Bridging the gap between top-down and bottom-up. Allan C. Wilson, 1934-1991. New Biol1991;3:911-913.
15.
Wallace D.: Mitochondrial genetics: A paradigm for aging and degenerative diseases?Science1992;256:628-632.