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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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Detaylı Bibliyografya
Asıl Yazarlar: Scheibye-Knudsen, Morten, Croteau, Deborah L., Bohr, Vilhelm A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
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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