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Results 1 - 2 of 2 for Combined oxidative phosphorylation defect type 15
  1. Combined oxidative phosphorylation deficiency 1 
    ... Testing Registry: Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 ... in the mitochondrial translation factor EFG1. Hum Mol Genet. 2006 Jun 1;15(11):1835-46. doi: 10.1093/hmg/ddl106. ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  2. RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy 
    ... essential for the process of energy production (called oxidative phosphorylation). The production of nucleotides by p53R2 helps maintain ...
    https://medlineplus.gov/...halomyopathic-form-with-renal-tubulopathy - Genetics