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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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Podrobná bibliografie
Vydáno v:Orphanet J Rare Dis
Hlavní autoři: Gehrig, Saskia Maria, Mihaylova, Violeta, Frese, Sebastian, Mueller, Sandro Manuel, Ligon-Auer, Maria, Spengler, Christina M., Petersen, Jens A., Lundby, Carsten, Jung, Hans H.
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
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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