Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01812849
Reference61 articles.
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3. Arts, W. F. M., Scholte, H. R., Loonen, M. C. B., Przyrembel, H., Fernandes, J., Trijbels, J. M. F. and Luyt-Houwen, I. E. M. Cytochromec oxidase deficiency in subacute necrotizing encephalomyelopathy.J. Neurol. Sci. 77 (1987) 103–115
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