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Genotyping possible polymorphic variants of human mismatch repair genes in healthy Korean individuals and sporadic colorectal cancer patients.

Familial cancer - 1 Jan 2004

Kim Jin C, Roh Seon A, Koo Kum H, Ka In H, Kim Hee C, Yu Chang S, Lee Kang H, Kim Jung S, Lee Han I, Bodmer Walter F

Abstract excerpt

The genotypic consequences of numerous single-nucleotide variants in human mismatch repair genes are mostly undetermined. We examined 27 reported single-nucleotide variants, rarely or ambiguously verified in a population-based study, to identify single-nucleotide polymorphisms (SNPs), haplotypes,...

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Share to Adaptor Proteins, Signal Transducing
Share to Base Pair Mismatch
Share to Colorectal Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Colorectal Neoplasms, Hereditary Nonpolyposis

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Identifiers

PMID: 15340264
DOI: 10.1023/B:FAME.0000039919.66461.8f

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15340264-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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