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Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNA(Met) 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension
To investigate the relationship between mitochondrial DNA (mtDNA) and hypertension as well as the mechanism involved in mitochondrial metabolic dysfunction. We identified a novel tRNA(Met) C4467A mutation in a Han Chinese family with hypertension. The maternal members presented with increased glucos...
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出版年: | Sci Rep |
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主要な著者: | , , , , , |
フォーマット: | Artigo |
言語: | Inglês |
出版事項: |
Nature Publishing Group UK
2017
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主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5465199/ https://ncbi.nlm.nih.gov/pubmed/28596595 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-03303-w |
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