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Results 1 - 10 of 11 for Mitochondrial complex I "deficiency," nuclear type 5
  1. Mitochondrial complex III deficiency 
    ... III deficiency nuclear type 4 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear type 5 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  2. Leigh syndrome 
    ... ClinicalTrials.gov NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5 LEIGH SYNDROME, NUCLEAR; NULS PubMed Ball M, ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  3. Mitochondrial complex V deficiency 
    ... their children. ATP synthase deficiency Genetic Testing Registry: Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B TMEM70-related mitochondrial encephalo-cardio-myopathy Isolated ...
    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 ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  5. BCS1L gene 
    ... mitochondrial complex III assembly Tests of BCS1L PubMed MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1; MC3DN1 BCS1 HOMOLOG, UBIQUINOL-CYTOCHROME C REDUCTASE ...
    https://medlineplus.gov/genetics/gene/bcs1l - Genetics
  6. 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
  7. MT-CYB gene 
    ... DNA is packaged in chromosomes within the nucleus (nuclear DNA), mitochondria also have a ... cause mitochondrial complex III deficiency. When caused by mutations in this gene, the ...
    https://medlineplus.gov/genetics/gene/mt-cyb - Genetics
  8. 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 ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  9. Talking Glossary of Genomic and Genetic Terms From the National Institutes of Health (National Human Genome Research Institute)  
    Genetic Testing/Reference Desk ... Genetic Testing ... Genetic Disorders/Reference Desk ... Genetic Disorders ... Birth Defects/Reference Desk ... Birth Defects ... Genes and Gene ...
    https://www.genome.gov/genetics-glossary - National Institutes of Health
  10. 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 - National Institutes of Health
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