Associated Papers
Translational and clinical comparison of whole genome and transcriptome to panel sequencing in precision oncology.
Kerle IA et al.
Npj Precision Oncology, 2025
Hypermutated phenotype in gliosarcoma of the spinal cord.
Hong CS et al.
Npj Precision Oncology, 2021
Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer.
Schubert SA et al.
Genes, Chromosomes & Cancer, 2020
32615015 (PubMed )
Supplement: GCC-59-697-s001.xlsx › S2_MSH6_MUTYH_patients
CoDP: predicting the impact of unclassified genetic variants in MSH6 by the combination of different properties of the protein.
Terui H et al.
Journal of Biomedical Science, 2013
MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer.
Giráldez MD et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2010
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