Mitochondrial complex I-linked disease
- 1 July 2016
- journal article
- Published by Elsevier BV in Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Vol. 1857 (7), 938-945
- https://doi.org/10.1016/j.bbabio.2016.02.012
Abstract
No abstract availableKeywords
This publication has 63 references indexed in Scilit:
- NDUFA4 Mutations Underlie Dysfunction of a Cytochrome c Oxidase Subunit Linked to Human Neurological DiseaseCell Reports, 2013
- Understanding mitochondrial complex I assembly in health and diseaseBiochimica et Biophysica Acta (BBA) - Bioenergetics, 2012
- Natural disease course and genotype‐phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 casesJournal of Inherited Metabolic Disease, 2012
- A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathyBrain, 2011
- Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporterNature, 2011
- A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporterNature, 2011
- Mitochondrial optic neuropathies – Disease mechanisms and therapeutic strategiesProgress in Retinal and Eye Research, 2011
- The sites and topology of mitochondrial superoxide productionExperimental Gerontology, 2010
- Biochemical diagnosis of mitochondrial disordersJournal of Inherited Metabolic Disease, 2010
- The antioxidant Trolox restores mitochondrial membrane potential and Ca2+-stimulated ATP production in human complex I deficiencyJournal of Molecular Medicine, 2009