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Impact of Different Selection Approaches for Identifying Lynch Syndrome-Related Colorectal Cancer Patients: Unity Is Strength
Lynch syndrome (LS) is an inherited genetic condition associated with increased predisposition to colorectal cancer (CRC) and other tumors and is caused by germline mutations in Mismatch Repair (MMR) or EPCAM genes. The identification of LS carriers is currently based on germline testing of subjects...
Autores principales: | Fanale, Daniele, Corsini, Lidia Rita, Brando, Chiara, Dimino, Alessandra, Filorizzo, Clarissa, Magrin, Luigi, Sciacchitano, Roberta, Fiorino, Alessia, Bazan Russo, Tancredi Didier, Calò, Valentina, Iovanna, Juan Lucio, Francini, Edoardo, Russo, Antonio, Bazan, Viviana |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864140/ https://www.ncbi.nlm.nih.gov/pubmed/35223509 http://dx.doi.org/10.3389/fonc.2022.827822 |
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