Characterisation of novel mutations in Cockayne syndrome type A and xeroderma pigmentosum group C subjects

A summary of mutations in the UV-sensiti

A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy

✍ James E. Cleaver; Larry H. Thompson; Audrey S. Richardson; J. Christopher States 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 393 KB 👁 1 views

The human diseases xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy are caused by mutations in a set of interacting gene products, which carry out the process of nucleotide excision repair. The majority of the genes have now been cloned and many mutations in the genes identified. Th