Mitochondrial DNA mutations in diseases of energy metabolism Douglas C. Wallace OriginalPaper Pages: 241 - 250
Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance Antonio TorroniDouglas C. Wallace OriginalPaper Pages: 261 - 271
Molecular basis of mitochondrial DNA disease Michael D. BrownDouglas C. Wallace OriginalPaper Pages: 273 - 289
Mitochondrial encephalomyopathies: Clinical and molecular analysis Eric A. SchonMichio HiranoSalvatore DiMauro OriginalPaper Pages: 291 - 299
Mitochondrial DNA diseases: Histological and cellular studies Eric A. Shoubridge OriginalPaper Pages: 301 - 310
MtDNA and nuclear mutations affecting oxidative phosphorylation: Correlating severity of clinical defect with extent of bioenergetic compromise B. H. Robinson OriginalPaper Pages: 311 - 316
Microcompartmentation of energy metabolism at the outer mitochondrial membrane: Role in diabetes mellitus and other diseases Edward R. B. McCabe OriginalPaper Pages: 317 - 325
Effects of amphipathic peptides, including presequences, on the functional integrity of rat liver mitochondrial membranes Klaas NicolayFanny Dorine LaterveerWaander Laurens van Heerde Original Articles Pages: 327 - 334
The role of Mg2+ in the hydrolytic activity of the isolated chloroplast ATPase: Study by high-performance liquid chromatography Gerard BergerGuy GiraultStephane Pezennec Original Articles Pages: 335 - 346
