QuickView for ORF20 (gene)

1. Mutations in the TTDN1 gene are associated with a distinct trichothiodystrophy phenotype.
2. A novel mutation in the C7orf11 gene causes nonphotosensitive trichothiodystrophy in a multiplex hig…
3. Pollitt syndrome patients carry mutation in TTDN1.
4. A functional link between lariat debranching enzyme and the intron-binding complex is defective in n…
5. Activation of human RNA lariat debranching enzyme Dbr1 by binding protein TTDN1 occurs though an int…

There were no clinical trials for ORF20