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Results 1 - 6 of 6 for Mitochondrial complex 1 "deficiency," nuclear type 11
  1. BCS1L gene 
    ... mitochondrial complex III assembly Tests of BCS1L ... by complex III: from mechanistic rationales to functional consequences. Biochim Biophys Acta. 2013 Nov-Dec;1827(11-12):1320-31. doi: 10.1016/j.bbabio. ...
    https://medlineplus.gov/genetics/gene/bcs1l - 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. Mitochondrial complex I deficiency 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1 PubMed Alston CL, Rocha MC, Lax NZ, ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  5. ACAD9 deficiency 
    ... I deficiency National Organization for Rare Disorders (NORD) MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20; MC1DN20 PubMed Aintablian HK, Narayanan V, Belnap ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  6. Combined oxidative phosphorylation deficiency 1 
    ... 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