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Neurobiology of Aging, ISSN 0197-4580, 2016, Volume 49, pp. 60 - 68
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 02/2007, Volume 16, Issue 4, pp. 431 - 444
Leigh syndrome associated with cytochrome c oxidase (COX) deficiency is a mitochondrial disorder usually caused by mutations of SURF1, a gene encoding a... 
CYTOCHROME-C-OXIDASE | OXIDATIVE-PHOSPHORYLATION | APOPTOSIS | ACID-INDUCED SEIZURES | BIOCHEMISTRY & MOLECULAR BIOLOGY | MITOCHONDRIA | CALCIUM | DISEASE | GENETICS & HEREDITY | PLASMA-MEMBRANE | EXPRESSION | DEFICIENCY
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JAMA Neurology, ISSN 2168-6149, 12/2016, Volume 73, Issue 12, pp. 1417 - 1424
Journal Article
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Journal of Neurology, ISSN 0340-5354, 3/2002, Volume 249, Issue 3, pp. 305 - 311
Journal Article