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Cytochrome-C-oxidase Deficiency in Muscles of a Floppy Infant Without Mitochondrial Myopathy

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Journal J Neurol
Specialty Neurology
Date 1982 Jan 1
PMID 6183406
Citations 18
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References
1.
Van Biervliet J, Bruinvis L, Ketting D, de Bree P, van der Heiden C, WADMAN S . Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles. Pediatr Res. 1977; 11(10 Pt 2):1088-93. DOI: 10.1203/00006450-197711100-00005. View

2.
Jerusalem F, Angelini C, Engel A, GROOVER R . Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy. Arch Neurol. 1973; 29(3):162-9. DOI: 10.1001/archneur.1973.00490270044007. View

3.
Hoppel C, Tomec R . Carnitine palmityltransferase. Location of two enzymatic activities in rat liver mitochondria. J Biol Chem. 1972; 247(3):832-41. View

4.
DiMauro S, Mendell J, Sahenk Z, Bachman D, Scarpa A, Scofield R . Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency. Neurology. 1980; 30(8):795-804. DOI: 10.1212/wnl.30.8.795. View

5.
Willems J, Monnens L, Trijbels J, Veerkamp J, MEYER A, van Dam K . Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue. Pediatrics. 1977; 60(6):850-7. View