SchapiraAHV. Inborn and induced defects of mitochondria. Arch Neurol1998;55:1293–1296.
8.
ChretienD, RustinP.Mitochondrial oxidative phosphorylation: pitfalls and tips in measuring and interpreting enzyme activities. J Inherit Metab Dis2003;26:189–198.
9.
ChretienD, GallegoJ, BarrientosA, Biochemical parameters for the diagnosis of mitochondrial respiratory chain deficiency in humans and their lack of age related changes. Biochem J1998;329:249–254.
10.
BrooksH, KraehenbuhlS.Development of a new assay for complex 1 of the respiratory chain. Clin Chem2000;46:345–350.
11.
HansonBJ, CapaldiRA, MarusschMF, SherwoodSW. An immunocytochemical approach to detection of mitochondrial disorders. J Histochem Cytochem2002;50:1281–1288.
12.
Rubio-GozalboME, DijkmanKP, VandenHeuvel LP, Clinical differences in patients with mitochondrio-cytopathies due to nuclear versus mitochondrial DNA mutations. Hum Mutat2000;15:522–532.
13.
DimauroS, SchoenEA. Mitochondrial DNA mutations in human disease. Am J Med Genet2001;106:18–26.