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The EMBO Journal, ISSN 0261-4189, 11/2004, Volume 23, Issue 23, pp. 4679 - 4689
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2018, Volume 176, Issue 2, pp. 399 - 403
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 03/2013, Volume 34, Issue 3, pp. 446 - 452
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 07/2018, Volume 115, Issue 27, pp. E6291 - E6300
Journal Article
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 2015, Volume 6, p. 134
Complex III (CIII) deficiency is one of the least common oxidative phosphorylation defects associated to mitochondrial disease. CIII constitutes the center of... 
Complex III deficiency | Mitochondrial diseases | Complex III assembly | Genetic mutations | Oxidative phosphorylation (OXPHOS) | Mitochondrial Diseases | oxidative phosphorylation (OXPHOS)
Journal Article
BBA - Molecular Cell Research, ISSN 0167-4889, 2009, Volume 1793, Issue 1, pp. 181 - 185
Complex III deficiencies are among the least common respiratory-chain abnormalities identified to date in humans. Nevertheless, their unexplained tissue... 
Mitochondria | QP-C | Cytochrome b | BC1 complex | Complex III | Human OXPHOS disease | BCS1L | MITOCHONDRIAL-DNA MUTATIONS | SUPEROXIDE | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISORDERS | SACCHAROMYCES-CEREVISIAE | CELL BIOLOGY | YEAST | ENCEPHALOPATHY | MAMMALIAN MITOCHONDRIA | BCS1L GENE | CYTOCHROME BC COMPLEX | OPTIC NEUROPATHY | Analysis | Mitochondrial DNA
Journal Article
Plos Genetics, ISSN 1553-7404, 2013, Volume 9, Issue 12, p. e1004034
Journal Article
BBA - Molecular Cell Research, ISSN 0167-4889, 12/2017, Volume 1864, Issue 12, pp. 2297 - 2307
Journal Article