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Article

Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition.

PLoS genetics - 1 Apr 2021

Nielsen Sofie V, Hartmann-Petersen Rasmus, Stein Amelie, Lindorff-Larsen Kresten

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Topics

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Share to Cancer Genomics and Diagnostics
Share to Colorectal Neoplasms, Hereditary Nonpolyposis
Share to DNA Mismatch Repair
Share to Genetic factors in colorectal cancer

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Mutation, Missense

Share to MutS Homolog 2 Protein

Share to Neoplasms

Source

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Identifiers

PMID: 33886538
DOI: 10.1371/journal.pgen.1009496
PMCID: PMC8061925

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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