Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
Titel:
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
Auteur:
Grolleman, Judith E. de Voer, Richarda M. Elsayed, Fadwa A. Nielsen, Maartje Weren, Robbert D.A. Palles, Claire Ligtenberg, Marjolijn J.L. Vos, Janet R. ten Broeke, Sanne W. de Miranda, Noel F.C.C. Kuiper, Renske A. Kamping, Eveline J. Jansen, Erik A.M. Vink-Börger, M. Elisa Popp, Isabell Lang, Alois Spier, Isabel Hüneburg, Robert James, Paul A. Li, Na Staninova, Marija Lindsay, Helen Cockburn, David Spasic-Boskovic, Olivera Clendenning, Mark Sweet, Kevin Capellá, Gabriel Sjursen, Wenche Høberg-Vetti, Hildegunn Jongmans, Marjolijn C. Neveling, Kornelia Geurts van Kessel, Ad Morreau, Hans Hes, Frederik J. Sijmons, Rolf H. Schackert, Hans K. Ruiz-Ponte, Clara Dymerska, Dagmara Lubinski, Jan Rivera, Barbara Foulkes, William D. Tomlinson, Ian P. Valle, Laura Buchanan, Daniel. D. Kenwrick, Sue Adlard, Julian Dimovski, Aleksandar J. Campbell, Ian G. Aretz, Stefan Schindler, Detlev van Wezel, Tom Hoogerbrugge, Nicoline Kuiper, Roland P.