Defects in mitochondrial respiratory complexes III and IV, and human pathologies

Author:

Borisov Vitaliy B

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry

Reference162 articles.

1. Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome;Adams;Ann. Neurol.,1997

2. Cyanide binding with ferricytochrome a3 in rat liver mitochondria;Andreev;Dokl. Acad. Nauk. SSSR,1979

3. Reaction of oxidized cytochrome oxidase with cyanide. Effects of pH, cytochrome c and membrane environment;Andreev;Bioorg. Khim.,1983

4. A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria;Andreu;Ann. Neurol.,1999

5. Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy;Andreu;Neurology,1998

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