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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...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2013
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| Gaiak: | |
| Sarrera elektronikoa: | 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 |
| Etiketak: |
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