University of Groningen
Correction
Dominguez-Valentin, Mev; Sampson, Julian R; Seppälä, Toni T; Ten Broeke, Sanne W;
Plazzer, John-Paul; Nakken, Sigve; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A; Sunde,
Lone
Published in:
Genetics in Medicine
DOI:
10.1038/s41436-020-0892-4
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Publication date:
2020
Link to publication in University of Groningen/UMCG research database
Citation for published version (APA):
Dominguez-Valentin, M., Sampson, J. R., Seppälä, T. T., Ten Broeke, S. W., Plazzer, J-P., Nakken, S.,
Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans,
D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos Tot Nederveen Cappel, W. H., ... Møller, P. (2020).
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants:
findings from the Prospective Lynch Syndrome Database. Genetics in Medicine, 22(9), 1569.
https://doi.org/10.1038/s41436-020-0892-4
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Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Mev Dominguez-Valentin, PhD , Julian R. Sampson, DM, FMedSci , Toni T. Seppälä, MD, PhD , Sanne W. ten Broeke, MD, PhD, John-Paul Plazzer, BE, Sigve Nakken, PhD, Christoph Engel, MD, Stefan Aretz, MD, Mark A. Jenkins, PhD, Lone Sunde, MD, PhD, Inge Bernstein, MD, PhD, Gabriel Capella, MD, Francesc Balaguer, MD, Huw Thomas, PhD, FRCP, D. Gareth Evans, MD FRCP, John Burn, MD, FMedSci, Marc Greenblatt, MD, Eivind Hovig, PhD, Wouter H. de Vos tot Nederveen Cappel, MD, Rolf H. Sijmons, MD, Lucio Bertario, MD, Maria Grazia Tibiletti, MD, Giulia Martina Cavestro, MD, Annika Lindblom, MD, Adriana Della Valle, MD, Francisco Lopez-Köstner, MD, PhD, Nathan Gluck, MD, PhD, Lior H. Katz, MD, Karl Heinimann, MD, PhD, Carlos A. Vaccaro, MD, Reinhard Büttner, MD, Heike Görgens, MD, Elke Holinski-Feder, MD, Monika Morak, PhD, Stefanie Holzapfel, MD,
Robert Hüneburg, MD, Magnus von Knebel Doeberitz, MD, Markus Loeffler, MD, Nils Rahner, MD, Hans K. Schackert, MD, Verena Steinke-Lange, MD, Wolff Schmiegel, MD, Deepak Vangala, MD, Kirsi Pylvänäinen, MD, Laura Renkonen-Sinisalo, MD, John L. Hopper, PhD, Aung Ko Win, PhD, Robert W. Haile, PhD, Noralane M. Lindor, MD, Steven Gallinger, MD, PhD, Loïc Le Marchand, PhD, Polly A. Newcomb, PhD, Jane C. Figueiredo, PhD, Stephen N. Thibodeau, PhD, Karin Wadt, MD, PhD, Christina Therkildsen, PhD, Henrik Okkels, PhD, Zohreh Ketabi, MD, PhD, Leticia Moreira, MD, Ariadna Sánchez, MD,
Miquel Serra-Burriel, PhD, Marta Pineda, PhD, Matilde Navarro, MD, Ignacio Blanco, MD, Kate Green, MD, Fiona Lalloo, MD, FRCP, Emma J. Crosbie, PhD, MRCOG, James Hill, MD, Oliver G. Denton, BSc, Ian M. Frayling, PhD, FRCPath,
Einar Andreas Rødland, PhD, MD, Hans Vasen, MD, Miriam Mints, MD, Florencia Neffa, MD, Patricia Esperon, PhD, Karin Alvarez, PhD, Revital Kariv, MD, Guy Rosner, MD, Tamara Alejandra Pinero, PhD, María Laura Gonzalez, MD, Pablo Kalfayan, MD,
Douglas Tjandra, MD, Ingrid M. Winship, MD, Finlay Macrae, MD, Gabriela Möslein, MD, Jukka-Pekka Mecklin, MD, Maartje Nielsen, MD, PhD and Pål Møller, MD
Genetics in Medicine (2020) https://doi.org/10.1038/s41436-020-0892-4
Correction to: Genetics in Medicine 22:2020;https://doi.org/10.1038/s41436-019-0596-9, published online 24 July 2019.
The original version of this Article did not contain details of Dutch Cancer Society (DCS) funding (grant number UL 2017-8223) in the Acknowledgements section. This has now been corrected in both the PDF and HTML versions of the Article.
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