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Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy
BACKGROUND: Mitochondrial myopathy severely affects skeletal muscle structure and function resulting in defective oxidative phosphorylation. However, the major pathomechanisms and therewith effective treatment approaches remain elusive. Therefore, the aim of the present study was to investigate dise...
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| Vydáno v: | Orphanet J Rare Dis |
|---|---|
| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4966582/ https://ncbi.nlm.nih.gov/pubmed/27473873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0488-x |
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