[Mitochondrial myopathy caused by complex III and IV deficiency. A familial case]

Authors :: M, Castro-Gago
I, Novo-Rodríguez
T, García Caballero
Y, Campos González
R, Huertas Barbero
J, Arenas Mora
Source :: Anales espanoles de pediatria. 38(1)
Publication Year :: 1993

Subjects :: Electron Transport Complex III
X Chromosome
Cytochrome-c Oxidase Deficiency
Humans
Mitochondrial Myopathies
Female
Child
Metabolism, Inborn Errors
Genes, Dominant
Mitochondria

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