1. Mitochondrial DNA mutations in diseases of energy metabolism

   • Douglas C. Wallace

   OriginalPaper Pages: 241 - 250

2. Mitochondrial DNA and human evolution

   • Mark Stoneking

   OriginalPaper Pages: 251 - 259

3. Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance

   • Antonio Torroni
   • Douglas C. Wallace

   OriginalPaper Pages: 261 - 271

4. Molecular basis of mitochondrial DNA disease

   • Michael D. Brown
   • Douglas C. Wallace

   OriginalPaper Pages: 273 - 289

5. Mitochondrial encephalomyopathies: Clinical and molecular analysis

   • Eric A. Schon
   • Michio Hirano
   • Salvatore DiMauro

   OriginalPaper Pages: 291 - 299

6. Mitochondrial DNA diseases: Histological and cellular studies

   • Eric A. Shoubridge

   OriginalPaper Pages: 301 - 310

7. MtDNA and nuclear mutations affecting oxidative phosphorylation: Correlating severity of clinical defect with extent of bioenergetic compromise

   • B. H. Robinson

   OriginalPaper Pages: 311 - 316

8. Microcompartmentation of energy metabolism at the outer mitochondrial membrane: Role in diabetes mellitus and other diseases

   • Edward R. B. McCabe

   OriginalPaper Pages: 317 - 325

9. Effects of amphipathic peptides, including presequences, on the functional integrity of rat liver mitochondrial membranes

   • Klaas Nicolay
   • Fanny Dorine Laterveer
   • Waander Laurens van Heerde

   Original Articles Pages: 327 - 334

10. The role of Mg²⁺ in the hydrolytic activity of the isolated chloroplast ATPase: Study by high-performance liquid chromatography

    • Gerard Berger
    • Guy Girault
    • Stephane Pezennec

    Original Articles Pages: 335 - 346