Disruption of TTDA results in complete nucleotide excision repair deficiency and embryonic lethality.
The ten-subunit transcription factor IIH (TFIIH) plays a crucial role in transcription and nucleotide excision repair (NER). Inactivating mutations in the smallest 8-kDa TFB5/TTDA subunit cause the neurodevelopmental progeroid repair syndrome trichothiodystrophy A (TTD-A). Previous studies have show...
Main Authors: | , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2013-04-01
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Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC3630102?pdf=render |