Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition

Half of the high-risk colorectal cancer families that fulfill the clinical criteria for Lynch syndrome lack germline mutations in the mismatch repair (MMR) genes and remain unexplained. Genetic testing for hereditary cancers is rapidly evolving due to the introduction of multigene panels, which may...

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Detalles Bibliográficos
Autores principales: Martin-Morales, Lorena, Rofes, Paula, Diaz-Rubio, Eduardo, Llovet, Patricia, Lorca, Victor, Bando, Inmaculada, Perez-Segura, Pedro, de la Hoya, Miguel, Garre, Pilar, Garcia-Barberan, Vanesa, Caldes, Trinidad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157886/
https://www.ncbi.nlm.nih.gov/pubmed/30256826
http://dx.doi.org/10.1371/journal.pone.0203885

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157886/
https://www.ncbi.nlm.nih.gov/pubmed/30256826
http://dx.doi.org/10.1371/journal.pone.0203885

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