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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...
में बचाया:
| मुख्य लेखकों: | , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
2013
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| विषय: | |
| ऑनलाइन पहुंच: | 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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