Associated Papers
Association of Inflammatory Mediators with Mitochondrial DNA Variants in Geriatric COVID-19 Patients.
Casoli T et al.
Aging and Disease, 2024
Pathogenic Biallelic Mutations in ECHS1 in a Case with Short-Chain Enoyl-CoA Hydratase (SCEH) Deficiency-Case Report and Literature Review.
Muntean C et al.
International Journal of Environmental Research and Public Health, 2022
Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes/Leigh syndrome overlap patient with a novel m.3482A>G mutation in MT-ND1.
Hayashi Y et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology, 2021
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