Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.
Forty per cent of patients with mitochondrial myopathies, a diverse group of multisystem diseases predominantly affecting skeletal muscle and the brain, have large deletions of a proportion of muscle mitochondrial DNA (mt DNA). These appeared to be identical in 13 of 28 cases, contained within the r...
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| 發表在: | Nucleic Acids Res |
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| Principais autores: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
1989
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| 在線閱讀: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC318006/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2748329/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/17.12.4465 |
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