Article
Characterization of molecular defects in xeroderma pigmentosum group C.
Nature genetics - 1 Dec 1993
Li L, Bales E S, Peterson C A, Legerski R J
Abstract excerpt
Xeroderma pigmentosum (XP) is a rare autosomal recessive disease of humans characterized by an accelerated chronic degeneration of sun-exposed areas of the body, including an elevated risk of developing cancers of the skin. We recently reported the isolation of a gene XPCC that complements the re...
Topics
- Base Sequence
- Blotting, Northern
- Cell Line
- DNA Mutational Analysis
- DNA Repair
- HeLa Cells
- Humans
- Molecular Sequence Data
- Mutation
- Xeroderma Pigmentosum