Zidovudine myopathy: A distinctive disorder associated with mitochondrial dysfunction
β Scribed by C. Mhiri; M. Baudrimont; G. Bonne; C. Geny; F. Degoul; C. Marsac; E. Roullet; Dr R. Gherardi
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 932 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
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## Paalman Transmitochondrial cybrid cell lines homoplasmic for the A8296G mtDNA transition, a mutation associated with several mitochondrial diseases, have a normal oxidative phosphorylation function, as shown by oxygen consumption, lactate production, respiratory enzyme activities, and growth usi