Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

Judith E. Grolleman, Richarda M. De Voer, Fadwa A. Elsayed, Maartje Nielsen, Robbert D.a. Weren, Claire Palles, Marjolijn J.l. Ligtenberg, Janet R. Vos, Sanne W. Ten Broeke, Noel F.c.c. De Miranda, Renske A. Kuiper, Eveline J. Kamping, Erik A.m. Jansen, M. Elisa Vink-börger, Isabell Popp, Alois Lang, Isabel Spier, Robert Hüneburg, Paul A. James, Na LiMarija Staninova, Helen Lindsay, David Cockburn, Olivera Spasic-boskovic, Mark Clendenning, Kevin Sweet, Gabriel Capellá, Wenche Sjursen, Hildegunn Høberg-vetti, Marjolijn C. Jongmans, Kornelia Neveling, Ad Geurts Van Kessel, Hans Morreau, Frederik J. Hes, Rolf H. Sijmons, Hans K. Schackert, Clara Ruiz-ponte, Dagmara Dymerska, Jan Lubinski, Barbara Rivera, William D. Foulkes, Ian P. Tomlinson, Laura Valle, Daniel. D. Buchanan, Sue Kenwrick, Julian Adlard, Aleksandar J. Dimovski, Ian G. Campbell, Stefan Aretz, Detlev Schindler, Tom Van Wezel, Nicoline Hoogerbrugge, Roland P. Kuiper

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)256-266.e5
JournalCancer Cell
Volume35
Issue number2
DOIs
Publication statusPublished - 11 Feb 2019

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