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Results 1 - 2 of 2 for Combined oxidative phosphorylation defect type 11
  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. Epub ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  2. RRM2B gene 
    ... that eye muscles are commonly affected by mitochondrial defects because they are especially ... combined with muscle weakness (encephalomyopathy) and a problem with ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics