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Results 1 - 6 of 6 for Mitochondrial complex 1 "deficiency," nuclear type 12
  1. BCS1L gene 
    ... mitochondrial complex III assembly Tests of ... 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.2012. ...
    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. ACAD9 deficiency 
    ... I deficiency National Organization for Rare Disorders (NORD) ... Mol Genet Metab Rep. 2016 Dec 29;10:38-44. doi: 10.1016/j.ymgmr.2016.12.005. eCollection 2017 Mar. Citation on PubMed or ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  5. Leigh syndrome 
    ... ClinicalTrials.gov NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5 LEIGH SYNDROME; LS PubMed Lake NJ, ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  6. Combined oxidative phosphorylation deficiency 1 
    ... elongation factor G1 function. As a result, fewer mitochondrial proteins ... phosphorylation deficiency 1 because it impairs the function of more than ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics