Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.

Authors Jenkins MA, Baglietto L, Dowty JG, et al.
Citation Clin Gastroenterol Hepatol. 2006 Apr;4(4):489-98.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16616355/
PMCID NA

Read this next

Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer.