Litcius/Paper detail

Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome

Christoph Engel, Aysel Ahadova, Toni T. Seppälä, Stefan Aretz, Marloes Bigirwamungu-Bargeman, Hendrik Bläker, Karolin Bucksch, Reinhard Büttner, Wouter T. de Vos tot Nederveen Cappel, Volker Endris, Elke Holinski‐Feder, Stefanie Holzapfel, Robert Hüneburg, Maarten Jacobs, Jan J. Koornstra, Alexandra M. J. Langers, Anna Lepistö, Monika Morak, Gabriela Möslein, Païvi Peltomäki, Kirsi Pylvänäinen, Nils Rahner, Laura Renkonen‐Sinisalo, Karsten Schulmann, Verena Steinke‐Lange, Albrecht Stenzinger, Christian P. Strassburg, Paul C. van de Meeberg, Mariëtte van Kouwen, Monique E. van Leerdam, Deepak Vangala, J. van der Vecht, Marie–Louise Verhulst, Magnus von Knebel Doeberitz, Jürgen Weitz, Silke Zachariae, Markus Loeffler, Jukka‐Pekka Mecklin, Matthias Kloor, Hans F. A. Vasen

2020Gastroenterology102 citationsDOIOpen Access PDF

Topics & Concepts

MSH6Lynch syndromeMLH1MSH2Somatic cellGermline mutationMedicineColorectal cancerInternal medicineOncologyMutationCancer researchDNA mismatch repairGeneticsBiologyGeneCancerGenetic factors in colorectal cancerMultiple and Secondary Primary CancersColorectal Cancer Screening and Detection