Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer
- PMID: 10682661
- PMCID: PMC2363304
- DOI: 10.1054/bjoc.1999.0959
Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer
Abstract
A polymorphism in hMSH2 gene has been associated with an increased susceptibility to develop colorectal cancer (CRC). Here we show that it is a genetic risk factor for CRC in the Spanish population. However, its presence does not apparently affect hMSH2 function.