Inactivation of DNA Mismatch Repair by Variants of Uncertain Significance in the PMS2 Gene
Author:
Affiliation:
1. Department of Toxicogenetics; Leiden University Medical Center; Leiden The Netherlands
Funder
NIH
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22426/fullpdf
Reference21 articles.
1. Mutational analysis of the PMS2 gene in sporadic endometrial cancers with microsatellite instability;Basil;Gynecol Oncol,1999
2. Refining the role of pms2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants;Borràs;J Med Genet,2013
3. Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial;Burn;Lancet,2011
4. Long-range PCR facilitates the identification of PMS2-specific mutations;Clendenning;Hum Mutat,2006
5. Genetic predisposition to colorectal cancer;Chapelle;Nat Rev Cancer,2004
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