1. Bootsma D, Kraemer KH, Cleaver JE et al. Nucleotide excision repair syndromes: xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Basis of Inherited Disease Vol. 1. New York: McGraw-Hill Book Co, 2001:677–703.
2. Friedberg EC, Walker GC, Siede W et al. DNA Repair and Mutagenesis, 2nd ed. Washington, DC: ASM Press, 2006.
3. Venema J, van Hoffen A, Karcagi V et al. Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes. Mol Cell Biol 1991;11:4128–4134.
4. Legerski R, Peterson C. Expression cloning of a human DNA repair gene involved in Xeroderma pigmentosum group C. Nature 1992;359:70–73.
5. Masutani C, Sugasawa K, Yanagisawa J et al. Purification and cloning of a nucleotide excision repair complex involving the Xeroderma pigmentosum group C protein and a human homolog of yeast RAD23. EMBO J 1994;13:1831–1843.