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PDF) UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases
PDF) A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation
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PDF) A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation
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UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases | Orphanet Journal of Rare Diseases | Full Text
UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases | Orphanet Journal of Rare Diseases | Full Text
PDF) A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation
