A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance—functional analysis reveals the pathogenic one

Overview of attention for article published in Familial Cancer, March 2011

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patent: 2 patents

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So far, Dimensions has found 4 publications that cite this research output.

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The most recent citing publications are shown below. View all 4 publications that cite this research output on Dimensions.

Tumor-independent Detection of Inherited Mismatch Repair Deficiency for the Diagnosis of Lynch Syndrome with High Specificity and Sensitivity

Article in Cancer Research Communications (March 2023)

Classification of MSH6 Variants of Uncertain Significance Using Functional Assays

Article in International Journal of Molecular Sciences (August 2021)

CoDP: predicting the impact of unclassified genetic variants in MSH6 by the combination of different properties of the protein

Article in Journal of Biomedical Science (April 2013)