Publication | Open Access

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNALEU(UUR) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)

Lactic AcidosisMitophagyMitochondrial BiogenesisMitochondrial FunctionGenetic DisorderGeneticsPathologyMitochondrial MedicineMolecular GeneticsMitochondrial EncephalomyopathyMitochondrial Point MutationMedicineCell Biology