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Published in 2019 at "Cell reports"
DOI: 10.1016/j.celrep.2019.09.028
Abstract: Cockayne syndrome (CS) is a rare genetic neurodevelopmental disorder, characterized by a deficiency in transcription-coupled subpathway of nucleotide excision DNA repair (TC-NER). Mutation of the Cockayne syndrome B (CSB) gene affects basal transcription, which is…
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Keywords:
cockayne syndrome;
model cockayne;
disease;
syndrome neurological ... See more keywords