Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome.

Raskin L, Schwenter F, Freytsis M, Tischkowitz M, Wong N, Chong G, Narod SA, Levine DA, Bogomolniy F, Aronson M, Thibodeau SN, Hunt KS, Rennert G, Gallinger S, Gruber SB, Foulkes WD
Clin Genet. 2011 79 (6): 512-22

PMID: 21155762 · PMCID: PMC4541773 · DOI:10.1111/j.1399-0004.2010.01594.x

MeSH Terms (23)

Adolescent Adult Aged Aged, 80 and over Case-Control Studies Colorectal Neoplasms, Hereditary Nonpolyposis DNA-Binding Proteins Endometrial Neoplasms Female Founder Effect Genetic Association Studies Genetic Markers Genetic Predisposition to Disease Haplotypes Humans INDEL Mutation Jews Male Middle Aged Odds Ratio Polymorphism, Single Nucleotide Sequence Analysis, DNA Young Adult

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