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Results 1 - 6 of 6 for Mitochondrial complex 1 "deficiency," nuclear type 15
  1. Mitochondrial complex III deficiency 
    ... Ubiquinone-cytochrome c oxidoreductase deficiency Genetic Testing Registry: Mitochondrial complex III deficiency nuclear type 1 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  2. Cytochrome c oxidase deficiency 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1; MC4DN1 MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 2; ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  3. Mitochondrial complex V deficiency 
    ... Rare Disorders (NORD) MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4B; MC5DN4B ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  4. BCS1L gene 
    ... mitochondrial complex III assembly Tests of BCS1L PubMed MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1; MC3DN1 BCS1 HOMOLOG, UBIQUINOL-CYTOCHROME C REDUCTASE COMPLEX ...
    https://medlineplus.gov/genetics/gene/bcs1l - Genetics
  5. Leigh syndrome 
    ... ClinicalTrials.gov NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT ... doi: 10.1002/ana.24551. Epub 2015 Dec 15. Citation on PubMed Pecina P, Capkova M, Chowdhury ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  6. Combined oxidative phosphorylation deficiency 1 
    ... Registry: Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 ... mutations 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