1. Mitochondrial encephalomyopathies;DiMauro;Arch. Neurol.,1993
2. J.A. Morgan-Hughes, Mitochondrial diseases, in: A.G. Engel, C. Franzini-Armstrong (Eds.), Myology, McGraw-Hill, New York, 1994, pp. 1610–1660.
3. J.M. Shoffner, D.C. Wallace, Oxidative-phosphorylation diseases, in: C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle (Eds.), Metabolic and Molecular Bases of Inherited Diseases, McGraw-Hill, New York, 1995, pp. 1535–1610.
4. Molecular genetic aspects of human mitochondrial disorders;Larsson;Annu. Rev. Genet.,1995
5. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency;Bourgeron;Nature Genet.,1995