Inherited deleterious variants inGALNT12are associated with CRC susceptibility
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22;Gray-McGuire;Cancer Res,2010
2. Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies;Green;Fam Cancer,2007
3. Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancers;Guda;Proc Natl Acad Sci USA,2009
4. Molecular cloning and characterization of a novel member of the UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase family, pp-GalNAc-T12;Guo;FEBS Lett,2002
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