Mechanistic Investigation on Mitochondrial Dysfunction and Apoptosis in mtDNA T8993G Mutation Cybrids
博士 === 國立清華大學 === 生物科技研究所 === 100 === Human mtDNA T8993G mutation is often fatal due to it inhibits significantly mitochondrial complex V (F1F0-ATPase) to cause severe ATP deficiency for clinically symptoms of neurological muscle weakness, ataxia, and retinitis pigmentosa (the so-called NARP mutatio...
| Main Authors: | , |
|---|---|
| Other Authors: | |
| Format: | Others |
| Language: | en_US |
| Published: |
2012
|
| Online Access: | http://ndltd.ncl.edu.tw/handle/25464493636426048190 |