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mfn2 protein human
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Hearts from 1d, 3wk, 5wk old mice overexpressing wildtype or mutant human MFN2
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MITOL-mediated DRP1 ubiquitylation and degradation promotes mitochondrial hyperfusion in a CMT2A-lin…
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy.
Mitofusin-2: Functional switch between mitochondrial function and neurodegeneration.
Optic atrophy in a patient with axonal Charcot-Marie-Tooth disease 2A2A due to MFN2 gene mutations].
From Cushing syndrome to lipodystrophy: an ultrarare case of MFN2-associated lipomatosis.
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Natural History Study of SLC25A46 Mutation-related Mitochondriopathy
Evaluation of Safety and Efficiency of Metreleptin Treatment for Patients With Multiple Symmetric Li…
MITAORTA - Role of Mitochondrial Dynamic in Aneurysm and Dissection of Ascending Thoracic Aorta
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