Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799245
Reference18 articles.
1. Bookelman, H., Trijibels, J. M. F., Sengers, R. C. A. and Janssen, A. J. M. Measurement of cytochromes in human skeletal muscle mitochondria isolated from fresh and frozen stored muscle specimens.Biochem. Med. 19 (1978) 366–373
2. Carafoli, E. and Roman, I. Mitochondria and disease.Mol. Aspects Med. 3 (1985) 295–429
3. DiMauro, S., Bonilla, E., Nakagawa, M. and DeVivo, D. Mitochondrial myopathies.Ann. Neurol. 17 (1985) 521–538
4. Hauswirth, W. W. and Laipis, P. J. Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows.Proc. Natl. Acad. Sci. USA 79 (1982) 4686–4690
5. Holt, I. J., Harding, A. E. and Morgan-Hughes, J. A. Deletion of muscle mitochondrial DNA in patients with mitochondrial myopathies.Nature (London) 331 (1988) 717–719
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