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Autor:
Tongling Liufu, Haiyan Yu, Jiaxi Yu, Meng Yu, Yue Tian, Yichun Ou, Jianwen Deng, Guogang Xing, Zhaoxia Wang
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Introduction: Mitochondrial disease is a spectrum of debilitating disorders caused by mutations in the mitochondrial DNA (mtDNA) or nuclear DNA that compromises the respiratory chain. Mitochondrial 3243A>G (m.3243 A>G) is the most common mutation sho
Externí odkaz:
https://doaj.org/article/e3a7952623c14f37874128394d6bcf4c
