Publication | Closed Access
Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
86
Citations
23
References
1991
Year
Mitochondrial MyopathyLactic AcidosisMendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsPathologyLeber Hereditary Optic NeuropathyMolecular GeneticsMedicineMitochondrial Dna Mutations
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