UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases | Orphanet Journal of Rare Diseases | Full Text
Activation of a cryptic splice site in the mitochondrial elongation factor GFM1 causes combined OXPHOS deficiency - ScienceDirect
UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases | Orphanet Journal of Rare Diseases | Full Text
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UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases | Orphanet Journal of Rare Diseases | Full Text
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PDF) A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation
UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases | Orphanet Journal of Rare Diseases | Full Text
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Activation of a cryptic splice site in the mitochondrial elongation factor GFM1 causes combined OXPHOS deficiency - ScienceDirect
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UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases | Orphanet Journal of Rare Diseases | Full Text
