Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic

Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic, also known as mitochondrial encephalomyopathy aminoacidopathy, is related to mitochondrial dna depletion syndrome 5 and suclg1-related mitochondrial dna depletion syndrome, encephalomyopathic form with methylmalonic aciduria. An important gene associated with Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic is SUCLA2 (Succinate-CoA Ligase ADP-Forming Subunit Beta). Affiliated tissues include brain and liver.