Article
MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology - 15 Oct 2001
Vasen H F, Stormorken A, Menko F H, Nagengast F M, Kleibeuker J H, Griffioen G, Taal B G, Moller P, Wijnen J T
Abstract excerpt
PURPOSE: Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disease characterized by the clustering of colorectal cancer, endometrial cancer, and various other cancers. The disease is caused by mutations in DNA-mismatch-repair (MMR) genes, most frequently in MLH1, MSH2, and MSH6. The aims of the present study were to compare the risk of developing colorectal, endometrial, and other cancers...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
