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

Author:

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.

Funder

COST

Dutch Cancer Society

Sacha Swarttouw-Hijmans Foundation

International Centre for Genetic Engineering and Biotechnology

Fondo de Investigacion Sanitaria

Schroeder-Kurth Fund

National Breast Cancer Foundation

Spanish Ministry of Economy and Competitiveness

FEDER

Deutsche Krebshilfe

Publisher

Elsevier BV

Subject

Cancer Research,Cell Biology,Oncology

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