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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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Autors principals: Scheibye-Knudsen, Morten, Croteau, Deborah L., Bohr, Vilhelm A.
Format: Artigo
Idioma:Inglês
Publicat: 2013
Matèries:
Accés en línia: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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