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1996, Oxford chemistry primers ; 40 Oxford ornithology series, ISBN 0198559046, Volume 40, 92
Book
The Sculpture Journal, ISSN 1366-2724, 01/2019, Volume 28, Issue 1, pp. 3 - 4
The articles in this issue continue Sculpture Journal's central aim to challenge traditional preconceptions by bringing into focus important new debates and... 
Sculpture
Journal Article
Sculpture Journal, ISSN 1366-2724, 01/2019, Volume 28, Issue 1, pp. 3 - 4
Journal Article
Journal Article
Journal Article
Plos Genetics, ISSN 1553-7404, 2013, Volume 9, Issue 12, p. e1004034
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 209 - 222
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Pathology, ISSN 0031-3025, 2014, Volume 46, pp. S25 - S26
Journal Article
JOURNAL OF BIOLOGICAL CHEMISTRY, ISSN 0021-9258, 04/2019, Volume 294, Issue 14, pp. 5386 - 5395
Inherited disorders of oxidative phosphorylation cause the clinically and genetically heterogeneous diseases known as mitochondrial energy generation... 
RECURRENT DE-NOVO | OXIDATIVE-PHOSPHORYLATION | COMPLEX | mitochondria | BIOCHEMISTRY & MOLECULAR BIOLOGY | OXPHOS | MEMBRANE-PROTEIN | ACYLGLYCEROL KINASE | mitochondrial disease | DEFICIENCY | SENGERS SYNDROME | genomics | genetic disease | respiratory chain | DNA MUTATIONS | NARP MUTATION | SUBUNIT | JBC Reviews
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Cell Metabolism, ISSN 1550-4131, 09/2011, Volume 14, Issue 3, pp. 428 - 434
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Journal Article
Human Mutation, ISSN 1059-7794, 07/2019, Volume 40, Issue 7, pp. 893 - 898
Leigh syndrome is a mitochondrial disease caused by pathogenic variants in over 85 genes. Whole exome sequencing of a patient with Leigh‐like syndrome... 
complex I | Leigh syndrome | TIMMDC1 | ACMG guidelines | protein truncation | MUTATION | GENETICS & HEREDITY | ASSOCIATION | MITOCHONDRIAL COMPLEX | Genetic research | Medical colleges | Genes | Medical genetics | Proteins | Mitochondria | Phenotypes | Diagnosis | Patients | Genomics
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