BRIEF RESEARCH REPORT
Published on 15 Oct 2025
A rare subtype of lynch syndrome familial with co-mutation of EpCAM c.344T>C, MSH2 c.2744A>G, PMS2 c.1408C>T and APC c.5465T>A, case report and literature review
doi 10.3389/fgene.2025.1667899
- 628 views
- Frontiers in Genetics
- Cancer Genetics and Oncogenomics
- Research Topics
- Unraveling Germline Mutations: Advances in Genetic Profiling for Cancer Risk
Unraveling Germline Mutations: Advances in Genetic Profiling for Cancer Risk
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