Identification and characterisation of a novel ubiquitylation site on Cockayne’s Syndrome B
Cockayne’s Syndrome is a rare hereditary disorder that is characterised by severe neurological abnormalities, cutaneous photosensitivity, severe growth failure and premature aging. The aetiology of this disorder is attributed to mutations and deletions in two proteins, Cockayne’s Syndrome A (CSA) an...
| Main Author: | |
|---|---|
| Published: |
University College London (University of London)
2014
|
| Subjects: | |
| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.626828 |