Cockayne Syndrome Group B Cellular and Biochemical Functions

The devastating genetic disorder Cockayne syndrome (CS) arises from mutations in the CSA and CSB genes. CS is characterized by progressive multisystem degeneration and is classified as a segmental premature-aging syndrome. The CS complementation group B (CSB) protein is at the interface of transcrip...

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Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Licht, Cecilie Löe, Stevnsner, Tinna, Bohr, Vilhelm A.
Materialtyp: Artigo
Språk:Inglês
Publicerad: The American Society of Human Genetics 2003
Ämnen:
Review Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1180389/
https://ncbi.nlm.nih.gov/pubmed/14639525
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