Assaying ATP synthesis in cultured cells: A valuable tool for the diagnosis of patients with mitochondrial disorders
- 22 May 2009
- journal article
- research article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 383 (1), 58-62
- https://doi.org/10.1016/j.bbrc.2009.03.121
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Cellular and functional analysis of four mutations located in the mitochondrial ATPase6 geneJournal of Cellular Biochemistry, 2009
- Pathogenic Mitochondrial DNA Mutations Are Common in the General PopulationAmerican Journal of Human Genetics, 2008
- Mitochondrial Mutations: Genotype to PhenotypePublished by Wiley ,2007
- COQ2 NephropathyJournal of the American Society of Nephrology, 2007
- Prevalence of mitochondrial DNA disease in adultsAnnals of Neurology, 2007
- Mitochondrial encephalomyopathies: an updateNeuromuscular Disorders, 2005
- The epidemiology of mitochondrial disorders—past, present and futureBiochimica et Biophysica Acta (BBA) - Bioenergetics, 2004
- Maternally‐inherited Leigh syndrome‐related mutations bolster mitochondrial‐mediated apoptosisJournal of Neurochemistry, 2004
- Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunitNeurology, 2003
- Pathogenesis of primary defects in mitochondrial ATP synthesisSeminars in Cell & Developmental Biology, 2001