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Transcription-coupled repair - mechanisms of action, regulation, and associated human disorders.
A Cockayne-Syndrome-Like Phenotype with a Homozygous Truncating UVSSA Variant: Might This Be a New Cause?
Differential processing of RNA polymerase II at DNA damage correlates with transcription-coupled repair syndrome severity.
A Homozygous Nonsense Variant in UVSSA Causes UV-sensitive Syndrome from Very Large Kindred: The First Report from Iran.
Epigenomic signature of accelerated ageing in progeroid Cockayne syndrome.