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A C. elegans homolog of the Cockayne syndrome complementation group A gene

Cockayne syndrome (CS) is a debilitating and complex disorder that result from inherited mutations in the CS complementation genes A and B, CSA and CSB. The links between the molecular functions of the CS genes and the complex pathophysiology of CS are as of yet poorly understood and are the subject...

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Detalles Bibliográficos
Publicado en:DNA Repair (Amst)
Main Authors: Babu, Vipin, Hofmann, Kay, Schumacher, Björn
Formato: Artigo
Idioma:Inglês
Publicado: 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4255241/
https://ncbi.nlm.nih.gov/pubmed/25453470
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dnarep.2014.09.011
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