T16189C mitochondrial DNA variant is associated with metabolic syndrome in Caucasian subjects
T16189C mitochondrial DNA variant is associated with metabolic syndrome in Caucasian subjects
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New York, NY: Elsevier Inc
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Language
English
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Publisher
New York, NY: Elsevier Inc
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Abstract Objectives Different nuclear genes are thought to be involved in the regulation of the complex phenotype of metabolic syndrome (MS) and their number is increasing. A mutation in mitochondrial DNA (mtDNA), T4291C in transfer RNA isoleucine (tRNAile), has been associated with MS in a large American family. In addition, a mtDNA T16189C varian...
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Full title
T16189C mitochondrial DNA variant is associated with metabolic syndrome in Caucasian subjects
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TN_cdi_proquest_miscellaneous_904487206
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_904487206
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ISSN
0899-9007
E-ISSN
1873-1244
DOI
10.1016/j.nut.2010.08.016
