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Results 1 - 10 of 11 for Mitochondrial complex 4 "deficiency," nuclear type 4
  1. Mitochondrial complex III deficiency 
    ... III deficiency nuclear type 3 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear type 4 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  2. Cytochrome c oxidase deficiency 
    ... fatal infantile, due to cytochrome c oxidase deficiency 4 Genetic Testing Registry: Cardioencephalomyopathy, fatal ... MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1; MC4DN1 MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  3. Mitochondrial complex V deficiency 
    ... Carrozzo R. TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesis. Neurogenetics. 2012 Nov;13(4):375-86. doi: 10.1007/s10048-012-0343-8. Epub 2012 Sep 18. Citation on PubMed
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  4. Mitochondrial complex I deficiency 
    ... Legrand A, Benit P, Rustin P, Slama A. Mitochondrial complex I deficiency of nuclear ... J Bioenerg Biomembr. 2014 Aug;46(4):323-8. doi: 10.1007/s10863-014-9564- ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  5. 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
  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. 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
  8. SDHA gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/sdha - Genetics
  9. 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 ... Genetic Counseling/ ...
    https://www.genome.gov/genetics-glossary - External Health Links
  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 - External Health Links
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