Identification of Lynch syndrome risk variants in the Romanian population

Two familial forms of colorectal cancer (CRC), Lynch syndrome (LS) and familial adenomatous polyposis (FAP), are caused by rare mutations in DNA mismatch repair genes (MLH1,MSH2,MSH6,PMS2) and the genes APC and MUTYH, respectively. No information is available on the presence of high‐risk CRC mutatio...

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Detalhes bibliográficos
Publicado no:J Cell Mol Med
Main Authors: Iordache, Paul D., Mates, Dana, Gunnarsson, Bjarni, Eggertsson, Hannes P., Sulem, Patrick, Benonisdottir, Stefania, Csiki, Irma Eva, Rascu, Stefan, Radavoi, Daniel, Ursu, Radu, Staicu, Catalin, Calota, Violeta, Voinoiu, Angelica, Jinga, Mariana, Rosoga, Gabriel, Danau, Razvan, Sima, Sorin Cristian, Badescu, Daniel, Suciu, Nicoleta, Radoi, Viorica, Mates, Ioan Nicolae, Dobra, Mihai, Nicolae, Camelia, Kristjansdottir, Sigrun, Jonasson, Jon G., Manolescu, Andrei, Arnadottir, Gudny, Jensson, Brynjar, Jonasdottir, Aslaug, Sigurdsson, Asgeir, le Roux, Louise, Johannsdottir, Hrefna, Rafnar, Thorunn, Halldorsson, Bjarni V., Jinga, Viorel, Stefansson, Kari
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6237568/
https://ncbi.nlm.nih.gov/pubmed/30324682
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.13881
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