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Results 1 - 10 of 10 for Mitochondrial complex 3 "deficiency," nuclear type 10
  1. Mitochondrial complex V deficiency 
    ... ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3; ... of mitochondrial disease. J Pathol. 2017 Jan;241(2):236-250. doi: 10.1002/path.4809. Epub 2016 Nov 2. Citation ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  2. Mitochondrial complex III deficiency 
    ... III deficiency nuclear type 2 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear type 3 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  3. Mitochondrial complex I deficiency 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov ... RW. The genetics and pathology of mitochondrial disease. J Pathol. 2017 Jan;241(2):236-250. doi: 10.1002/path.4809. Epub 2016 Nov 2. Citation ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  4. Cytochrome c oxidase deficiency 
    ... fatal infantile, due to cytochrome c oxidase deficiency 3 Genetic Testing Registry: Cardioencephalomyopathy, fatal ... COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1; MC4DN1 MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  5. ACAD9 deficiency 
    ... I deficiency National Organization for Rare Disorders (NORD) ... the phenotypic spectrum and alters treatment approach. Mol Genet Metab Rep. 2016 Dec 29;10:38-44. doi: 10.1016/j.ymgmr.2016. ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  6. SDHA gene 
    ... SDH1 SDH2 SDHF succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial succinate dehydrogenase complex flavoprotein ... gastrointestinal stromal tumors. Front Oncol. 2013 May 17;3:117. doi: 10.3389/fonc.2013.00117. eCollection 2013. Citation on ...
    https://medlineplus.gov/genetics/gene/sdha - Genetics
  7. Leigh syndrome 
    ... ClinicalTrials.gov NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5 LEIGH SYNDROME, NUCLEAR; NULS PubMed Ball ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  8. Combined oxidative phosphorylation deficiency 1 
    ... den Heuvel LP. Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle. Eur J Hum Genet. 2011 Mar;19(3):275-9. doi: 10.1038/ejhg.2010.208. Epub 2010 Dec 1. ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  9. Parkinson's Disease From the National Institutes of Health (National Institute of Environmental Health Sciences)  
    Parkinson's Disease/Statistics and Research ... Parkinson's Disease ... National Institute of Environmental Health Sciences ... From the National Institutes of Health
    https://www.niehs.nih.gov/health/topics/conditions/parkinson - External Health Links
  10. Research Ethics Timeline From the National Institutes of Health (National Institute of Environmental Health Sciences)  
    Medical Ethics/Learn More ... Medical Ethics ... National Institute of Environmental Health Sciences ... From the National Institutes of Health ... A research ethics timeline ...
    https://www.niehs.nih.gov/research/resources/bioethics/timeline - External Health Links