fig2
![Advancement in the diagnosis of mitochondrial diseases](https://image.oaes.cc/078bc05b-ba95-42ac-ad6f-fc0bb16e3e13/3508.fig.2.jpg)
Figure 2. Common diseases associated with mtDNA mutations and the genes involved[24]. LHON: leber hereditary optic neuropathy; CPEO: chronic progressive external ophthalmoplegia; MERRF: myoclonic epilepsy with ragged-red fibers; MND: motor neuron disease; MELAS: mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes; PD: Parkinson’s disease