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Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: A cybrid study

Metabolic SyndromeCardiomyopathyMetabolic DisorderMitochondrial FunctionGeneticsPhysiologyDiabetesType 2Diabetes MellitusMedicineCybrid StudyHealth Sciences