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Nature, ISSN 0028-0836, 12/2017, Volume 552, Issue 7684, pp. 273 - 277
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 12/2018, Volume 63, Issue 12, pp. 1269 - 1272
Leigh syndrome is one of the most common subtypes of mitochondrial disease. Mutations in encoding genes of oxidative phosphorylation complexes have been... 
GENETICS & HEREDITY | Asian Continental Ancestry Group | Humans | Infant | Male | NADH Dehydrogenase - genetics | Mutation, Missense | Leigh Disease - genetics | Mutation
Journal Article
Journal Article
Diabetes, ISSN 0012-1797, 07/2018, Volume 67, Issue 7, pp. 1441 - 1453
Mitochondrial DNA (mtDNA) haplogroups have been associated with the incidence of type 2 diabetes (T2D); however, their underlying role in T2D remains poorly... 
INSULIN | CELLS | POPULATION | REDOX STATE | DISEASE | ENDOCRINOLOGY & METABOLISM | RESISTANCE | HEREDITARY OPTIC NEUROPATHY | DNA VARIANTS | HAN CHINESE | ASSOCIATION | Type 2 diabetes | Mitochondrial DNA | Research | Diagnosis | Risk factors
Journal Article
Journal Article
Nature Cell Biology, ISSN 1465-7392, 10/2015, Volume 17, Issue 10, pp. 1348 - 1355
Journal Article
International Journal of Cancer, ISSN 0020-7136, 05/2018, Volume 142, Issue 9, pp. 1786 - 1796
Journal Article