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Results 1 - 8 of 8 for Mitochondrial complex 1 "deficiency," nuclear type 19
  1. ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1; MC4DN1 MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 2; ...
  2. ... Rare Disorders (NORD) MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4B; MC5DN4B ...
  3. ... mitochondrial complex III assembly Tests of BCS1L PubMed MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1; MC3DN1 BCS1 HOMOLOG, UBIQUINOL-CYTOCHROME C REDUCTASE COMPLEX ...
  4. ... elongation factor G1 function. As a result, fewer mitochondrial proteins ... phosphorylation deficiency 1 because it impairs the function of more than ...
  5. ... SDH1 SDH2 SDHF succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial succinate dehydrogenase complex flavoprotein ... Belinsky MG, Rink L, von Mehren M. Succinate dehydrogenase deficiency in pediatric and adult gastrointestinal stromal tumors. Front ...
  6. 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
  7. 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 ...
  8. Talking Glossary of Genetic Terms From the National Institutes of Health (National Human Genome Research Institute)  
    Genetic Disorders/Reference Desk ... Genetic Disorders ... Genetic Testing/Reference Desk ... Genetic Testing ... Birth Defects/Reference Desk ... Birth Defects ... Genes and Gene ...