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Results 1 - 5 of 5 for Leigh Syndrome nuclear DNA mutation
Did you mean light Syndrome nuclear DNA mutation?
  1. MT-ND5 gene 
    ... MT-ND5 PubMed COMPLEX ... Vincent-Delorme C, Cormier-Daire V, Rustin P, Rotig A, Munnich A. The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a ...
    https://medlineplus.gov/genetics/gene/mt-nd5 - Genetics
  2. MT-TV gene 
    ... Thomas NH, Harding AE, Hammans SR. A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome. Neurology. 1997 Aug;49(2):589-92. doi: ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  3. MT-ND6 gene 
    ... Kahler SG, Freckmann ML, Reddihough D, Thorburn DR. Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families. Ann Neurol. 2000 Jul;48( ...
    https://medlineplus.gov/genetics/gene/mt-nd6 - Genetics
  4. GFM1 gene 
    ... that is stored in the nucleus of cells (nuclear DNA), a few proteins and other molecules are produced ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health ... tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1. Hum Mol ...
    https://medlineplus.gov/genetics/gene/gfm1 - Genetics
  5. BCS1L gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This ... MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1; MC3DN1 BCS1 HOMOLOG, UBIQUINOL-CYTOCHROME C ...
    https://medlineplus.gov/genetics/gene/bcs1l - Genetics