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Mitochondrial deficiency in Cockayne syndrome
Cockayne syndrome is a rare inherited disorder characterized by accelerated aging, cachectic dwarfism and many other features. Recent work has implicated mitochondrial dysfunction in the pathogenesis of this disease. This is particularly interesting since mitochondrial deficiencies are believed to b...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3663877/ https://ncbi.nlm.nih.gov/pubmed/23435289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mad.2013.02.007 |
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