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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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Bibliografiske detaljer
Main Authors: Scheibye-Knudsen, Morten, Croteau, Deborah L., Bohr, Vilhelm A.
Format: Artigo
Sprog:Inglês
Udgivet: 2013
Fag:
Online adgang: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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